chr6:33026246:A>G Detail (hg19)

Information

Genome

Assembly Position
hg19 chr6:33,026,246-33,026,246
hg38 chr6:33,058,469-33,058,469 View the variant detail on this assembly version.

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.610
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
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
not provided hepatitis B MGS000002
(TMGS000002)
Masashi Mizokami National Center for Global Health and Medicine
not provided biliary cirrhosis, primary not provided MGS000089
(TMGS000168)
Minoru Nakamura
Minoru Nakamura
National Hospital Organization Nagasaki Medical Center
National Hospital Organization Nagasaki Medical Center
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.248 Hepatitis B, Chronic [Strong influence of human leukocyte antigen (HLA)-DP gene variants on developme... GAD 21274863 Detail
0.132 hepatitis B By using logistic regression analysis, these two SNPs in the HLA-DPA1 and HLA-DP... BeFree 21904616 Detail
0.123 hepatitis B By using logistic regression analysis, these two SNPs in the HLA-DPA1 and HLA-DP... BeFree 21904616 Detail
Annotation

Annotations

DescrptionSourceLinks
[Strong influence of human leukocyte antigen (HLA)-DP gene variants on development of persistent chr... DisGeNET Detail
By using logistic regression analysis, these two SNPs in the HLA-DPA1 and HLA-DPB1 genes were signif... DisGeNET Detail
By using logistic regression analysis, these two SNPs in the HLA-DPA1 and HLA-DPB1 genes were signif... DisGeNET Detail
Gene
-
dbSNP
rs2395309 dbSNP
Genome
hg19
Position
chr6:33,026,246-33,026,246
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))
rs2395309
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.61
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
10224
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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