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rs12032814

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs12032814(A;A)
Make rs12032814(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position9247171
GeneH6PD
is asnp
is mentioned by
dbSNPrs12032814
ebirs12032814
HLIrs12032814
Exacrs12032814
Varsomers12032814
Maprs12032814
PheGenIrs12032814
hapmaprs12032814
1000 genomesrs12032814
hgdprs12032814
ensemblrs12032814
gopubmedrs12032814
geneviewrs12032814
scholarrs12032814
googlers12032814
pharmgkbrs12032814
gwascentralrs12032814
openSNPrs12032814
23andMers12032814
23andMe allrs12032814
SNP Nexus

SNPshotrs12032814
SNPdbers12032814
MSV3drs12032814
GWAS Ctlgrs12032814
Max Magnitude0
ClinVar
Risk rs12032814(A;A)
Alt rs12032814(A;A)
Reference rs12032814(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene H6PD
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.9307230T>A
CLNSRC
CLNACC RCV000171451.1,