chr6:32698518:A>G Detail (hg38)

Information

Genome

Assembly Position
hg19 chr6:32,666,295-32,666,295 View the variant detail on this assembly version.
hg38 chr6:32,698,518-32,698,518

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.258
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 Hepatitis B Virus-Related Hepatocellular Carcinoma Genome-wide association studies (GWAS) have identified three loci (rs17401966 in... BeFree 24204805 Detail
<0.001 Hepatitis B Virus-Related Hepatocellular Carcinoma Genome-wide association studies (GWAS) have identified three loci (rs17401966 in... BeFree 24204805 Detail
0.001 hepatitis B Genome-wide association studies (GWAS) have identified three loci (rs17401966 in... BeFree 24204805 Detail
0.011 hepatitis B Genome-wide association studies (GWAS) have identified three loci (rs17401966 in... BeFree 24204805 Detail
<0.001 Hepatitis B Virus-Related Hepatocellular Carcinoma Genome-wide association studies (GWAS) have identified three loci (rs17401966 in... BeFree 24204805 Detail
<0.001 hepatitis C Genome-wide association studies (GWAS) have identified three loci (rs17401966 in... BeFree 24204805 Detail
<0.001 Hepatitis B Virus-Related Hepatocellular Carcinoma Genome-wide association studies (GWAS) have identified three loci (rs17401966 in... BeFree 24204805 Detail
<0.001 hepatitis C Genome-wide association studies (GWAS) have identified three loci (rs17401966 in... BeFree 24204805 Detail
<0.001 Hepatitis B Virus-Related Hepatocellular Carcinoma Genome-wide association studies (GWAS) have identified three loci (rs17401966 in... BeFree 24204805 Detail
0.032 hepatitis C Genome-wide association studies (GWAS) have identified three loci (rs17401966 in... BeFree 24204805 Detail
0.004 hepatitis C Genome-wide association studies (GWAS) have identified three loci (rs17401966 in... BeFree 24204805 Detail
0.001 hepatitis B Genome-wide association studies (GWAS) have identified three loci (rs17401966 in... BeFree 24204805 Detail
Annotation

Annotations

DescrptionSourceLinks
Genome-wide association studies (GWAS) have identified three loci (rs17401966 in KIF1B, rs7574865 in... DisGeNET Detail
Genome-wide association studies (GWAS) have identified three loci (rs17401966 in KIF1B, rs7574865 in... DisGeNET Detail
Genome-wide association studies (GWAS) have identified three loci (rs17401966 in KIF1B, rs7574865 in... DisGeNET Detail
Genome-wide association studies (GWAS) have identified three loci (rs17401966 in KIF1B, rs7574865 in... DisGeNET Detail
Genome-wide association studies (GWAS) have identified three loci (rs17401966 in KIF1B, rs7574865 in... DisGeNET Detail
Genome-wide association studies (GWAS) have identified three loci (rs17401966 in KIF1B, rs7574865 in... DisGeNET Detail
Genome-wide association studies (GWAS) have identified three loci (rs17401966 in KIF1B, rs7574865 in... DisGeNET Detail
Genome-wide association studies (GWAS) have identified three loci (rs17401966 in KIF1B, rs7574865 in... DisGeNET Detail
Genome-wide association studies (GWAS) have identified three loci (rs17401966 in KIF1B, rs7574865 in... DisGeNET Detail
Genome-wide association studies (GWAS) have identified three loci (rs17401966 in KIF1B, rs7574865 in... DisGeNET Detail
Genome-wide association studies (GWAS) have identified three loci (rs17401966 in KIF1B, rs7574865 in... DisGeNET Detail
Genome-wide association studies (GWAS) have identified three loci (rs17401966 in KIF1B, rs7574865 in... DisGeNET Detail
Gene
-
dbSNP
rs9275319 dbSNP
Genome
hg38
Position
chr6:32,698,518-32,698,518
Variant Type
snv
Reference Allele
A
Alternative Allele
G
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs9275319
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.2579
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
4323
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
Genome browser