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rs786204677

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204677(A;A)
Make rs786204677(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position19657867
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs786204677
ebirs786204677
HLIrs786204677
Exacrs786204677
Varsomers786204677
Maprs786204677
PheGenIrs786204677
hapmaprs786204677
1000 genomesrs786204677
hgdprs786204677
ensemblrs786204677
gopubmedrs786204677
geneviewrs786204677
scholarrs786204677
googlers786204677
pharmgkbrs786204677
gwascentralrs786204677
openSNPrs786204677
23andMers786204677
23andMe allrs786204677
SNP Nexus

SNPshotrs786204677
SNPdbers786204677
MSV3drs786204677
GWAS Ctlgrs786204677
Max Magnitude0
ClinVar
Risk rs786204677(A;A)
Alt rs786204677(A;A)
Reference rs786204677(G;G)
Significance Probable-Pathogenic
Disease Sjögren-Larsson syndrome
Variation info
Gene ALDH3A2
CLNDBN Sjögren-Larsson syndrome
Reversed 0
HGVS NC_000017.10:g.19561180G>A
CLNSRC
CLNACC RCV000169484.1,