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rs201458895

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs201458895(C;C)
Make rs201458895(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position38396512
GeneALDH1B1
is asnp
is mentioned by
dbSNPrs201458895
ebirs201458895
HLIrs201458895
Exacrs201458895
Varsomers201458895
Maprs201458895
PheGenIrs201458895
hapmaprs201458895
1000 genomesrs201458895
hgdprs201458895
ensemblrs201458895
gopubmedrs201458895
geneviewrs201458895
scholarrs201458895
googlers201458895
pharmgkbrs201458895
gwascentralrs201458895
openSNPrs201458895
23andMers201458895
23andMe allrs201458895
SNP Nexus

SNPshotrs201458895
SNPdbers201458895
MSV3drs201458895
GWAS Ctlgrs201458895
Max Magnitude0
ClinVar
Risk rs201458895(C;C)
Alt rs201458895(C;C)
Reference rs201458895(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALDH1B1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.38396509T>C
CLNSRC
CLNACC RCV000196411.1,