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rs786205501

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205501(C;C)
Make rs786205501(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position19656517
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs786205501
ebirs786205501
HLIrs786205501
Exacrs786205501
Varsomers786205501
Maprs786205501
PheGenIrs786205501
hapmaprs786205501
1000 genomesrs786205501
hgdprs786205501
ensemblrs786205501
gopubmedrs786205501
geneviewrs786205501
scholarrs786205501
googlers786205501
pharmgkbrs786205501
gwascentralrs786205501
openSNPrs786205501
23andMers786205501
23andMe allrs786205501
SNP Nexus

SNPshotrs786205501
SNPdbers786205501
MSV3drs786205501
GWAS Ctlgrs786205501
Max Magnitude0
ClinVar
Risk rs786205501(C;C)
Alt rs786205501(C;C)
Reference rs786205501(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALDH3A2
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.19559830T>C
CLNSRC
CLNACC RCV000171251.1,