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rs398122931

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122931(A;A)
Make rs398122931(A;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position12884903
GeneKLF1
is asnp
is mentioned by
dbSNPrs398122931
ebirs398122931
HLIrs398122931
Exacrs398122931
Varsomers398122931
Maprs398122931
PheGenIrs398122931
hapmaprs398122931
1000 genomesrs398122931
hgdprs398122931
ensemblrs398122931
gopubmedrs398122931
geneviewrs398122931
scholarrs398122931
googlers398122931
pharmgkbrs398122931
gwascentralrs398122931
openSNPrs398122931
23andMers398122931
23andMe allrs398122931
SNP Nexus

SNPshotrs398122931
SNPdbers398122931
MSV3drs398122931
GWAS Ctlgrs398122931
Max Magnitude0
ClinVar
Risk rs398122931(A,T;A,T)
Alt rs398122931(A,T;A,T)
Reference rs398122931(C;C)
Significance Pathogenic
Disease BLOOD GROUP--LUTHERAN INHIBITOR
Variation info
Gene KLF1
CLNDBN BLOOD GROUP--LUTHERAN INHIBITOR
Reversed 1
HGVS NC_000019.9:g.12995717G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033156.4,