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rs121908986

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121908986(C;C)
Make rs121908986(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position165683019
GeneALDH9A1
is asnp
is mentioned by
dbSNPrs121908986
ebirs121908986
HLIrs121908986
Exacrs121908986
Varsomers121908986
Maprs121908986
PheGenIrs121908986
hapmaprs121908986
1000 genomesrs121908986
hgdprs121908986
ensemblrs121908986
gopubmedrs121908986
geneviewrs121908986
scholarrs121908986
googlers121908986
pharmgkbrs121908986
gwascentralrs121908986
openSNPrs121908986
23andMers121908986
23andMe allrs121908986
SNP Nexus

SNPshotrs121908986
SNPdbers121908986
MSV3drs121908986
GWAS Ctlgrs121908986
Max Magnitude0
OMIM602733
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908986(A,C;A,C)
Alt rs121908986(A,C;A,C)
Reference rs121908986(G;G)
Significance Other
Disease ALDH9A1*2 POLYMORPHISM
Variation info
Gene ALDH9A1
CLNDBN ALDH9A1*2 POLYMORPHISM
Reversed 1
HGVS NC_000001.10:g.165652256C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007260.3,