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rs779869631

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs779869631(C;C)
Make rs779869631(C;G)
ReferenceGRCh38.p7 38.3/149
Chromosome7
Position138762983
GeneATP6V0A4
is asnp
is mentioned by
dbSNPrs779869631
dbSNP (classic)rs779869631
ClinGenrs779869631
ebirs779869631
HLIrs779869631
Exacrs779869631
Gnomadrs779869631
Varsomers779869631
LitVarrs779869631
Maprs779869631
PheGenIrs779869631
Biobankrs779869631
1000 genomesrs779869631
hgdprs779869631
ensemblrs779869631
geneviewrs779869631
scholarrs779869631
googlers779869631
pharmgkbrs779869631
gwascentralrs779869631
openSNPrs779869631
23andMers779869631
23andMe allrs779869631
SNPshotrs779869631
SNPdbers779869631
MSV3drs779869631
GWAS Ctlgrs779869631
Max Magnitude0
ClinVar
Risk rs779869631(A;A) rs779869631(C;C)
Alt rs779869631(A;A) rs779869631(C;C)
Reference Rs779869631(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ATP6V0A4
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.138447728G>A
CLNSRC
CLNACC RCV000287838.1,