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rs376526037

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs376526037(A;A)
Make rs376526037(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position49483504
GeneERCC6
is asnp
is mentioned by
dbSNPrs376526037
dbSNP (classic)rs376526037
ClinGenrs376526037
ebirs376526037
HLIrs376526037
Exacrs376526037
Gnomadrs376526037
Varsomers376526037
LitVarrs376526037
Maprs376526037
PheGenIrs376526037
Biobankrs376526037
1000 genomesrs376526037
hgdprs376526037
ensemblrs376526037
geneviewrs376526037
scholarrs376526037
googlers376526037
pharmgkbrs376526037
gwascentralrs376526037
openSNPrs376526037
23andMers376526037
23andMe allrs376526037
SNPshotrs376526037
SNPdbers376526037
MSV3drs376526037
GWAS Ctlgrs376526037
Max Magnitude0
ClinVar
Risk rs376526037(A;A)
Alt rs376526037(A;A)
Reference Rs376526037(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ERCC6
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.50691550G>A
CLNSRC
CLNACC RCV000494216.1,