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rs397514634

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397514634(G;G)
Make rs397514634(G;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position12884997
GeneKLF1
is asnp
is mentioned by
dbSNPrs397514634
ebirs397514634
HLIrs397514634
Exacrs397514634
Varsomers397514634
Maprs397514634
PheGenIrs397514634
hapmaprs397514634
1000 genomesrs397514634
hgdprs397514634
ensemblrs397514634
gopubmedrs397514634
geneviewrs397514634
scholarrs397514634
googlers397514634
pharmgkbrs397514634
gwascentralrs397514634
openSNPrs397514634
23andMers397514634
23andMe allrs397514634
SNP Nexus

SNPshotrs397514634
SNPdbers397514634
MSV3drs397514634
GWAS Ctlgrs397514634
Max Magnitude0
ClinVar
Risk rs397514634(C,G;C,G)
Alt rs397514634(C,G;C,G)
Reference rs397514634(T;T)
Significance Pathogenic
Disease BLOOD GROUP--LUTHERAN INHIBITOR
Variation info
Gene KLF1
CLNDBN BLOOD GROUP--LUTHERAN INHIBITOR
Reversed 1
HGVS NC_000019.9:g.12995811A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000033155.4,