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rs142427338

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs142427338(C;T)
Make rs142427338(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position38396880
GeneALDH1B1
is asnp
is mentioned by
dbSNPrs142427338
ebirs142427338
HLIrs142427338
Exacrs142427338
Varsomers142427338
Maprs142427338
PheGenIrs142427338
hapmaprs142427338
1000 genomesrs142427338
hgdprs142427338
ensemblrs142427338
gopubmedrs142427338
geneviewrs142427338
scholarrs142427338
googlers142427338
pharmgkbrs142427338
gwascentralrs142427338
openSNPrs142427338
23andMers142427338
23andMe allrs142427338
SNP Nexus

SNPshotrs142427338
SNPdbers142427338
MSV3drs142427338
GWAS Ctlgrs142427338
Max Magnitude0
ClinVar
Risk rs142427338(T;T)
Alt rs142427338(T;T)
Reference rs142427338(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ALDH1B1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.38396877C>T
CLNSRC
CLNACC RCV000200827.1,