chr10:69643342:T>C Detail (hg19)

Information

Genome

Assembly Position
hg19 chr10:69,643,342-69,643,342
hg38 chr10:67,883,584-67,883,584 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:0.179
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 Metabolic syndrome X Nominally significant associations were also observed between T2D and the SIRT1 ... BeFree 20503258 Detail
0.211 Diabetes Mellitus, Non-Insulin-Dependent Nominally significant associations were also observed between T2D and the SIRT1 ... BeFree 20503258 Detail
0.204 Metabolic syndrome X Nominally significant associations were also observed between T2D and the SIRT1 ... BeFree 20503258 Detail
Annotation

Annotations

DescrptionSourceLinks
Nominally significant associations were also observed between T2D and the SIRT1 rs3758391 SNP and MS... DisGeNET Detail
Nominally significant associations were also observed between T2D and the SIRT1 rs3758391 SNP and MS... DisGeNET Detail
Nominally significant associations were also observed between T2D and the SIRT1 rs3758391 SNP and MS... DisGeNET Detail
Gene
-
dbSNP
rs3758391 dbSNP
Genome
hg19
Position
chr10:69,643,342-69,643,342
Variant Type
snv
Reference Allele
T
Alternative Allele
C
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))
rs3758391
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.1792
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
3003
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
Genome browser