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rs137852688

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852688(C;T)
Make rs137852688(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position12885335
GeneKLF1
is asnp
is mentioned by
dbSNPrs137852688
ebirs137852688
HLIrs137852688
Exacrs137852688
Varsomers137852688
Maprs137852688
PheGenIrs137852688
hapmaprs137852688
1000 genomesrs137852688
hgdprs137852688
ensemblrs137852688
gopubmedrs137852688
geneviewrs137852688
scholarrs137852688
googlers137852688
pharmgkbrs137852688
gwascentralrs137852688
openSNPrs137852688
23andMers137852688
23andMe allrs137852688
SNP Nexus

SNPshotrs137852688
SNPdbers137852688
MSV3drs137852688
GWAS Ctlgrs137852688
Max Magnitude0
OMIM600599
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137852688(G,T;G,T)
Alt rs137852688(G,T;G,T)
Reference rs137852688(C;C)
Significance Pathogenic
Disease BLOOD GROUP--LUTHERAN INHIBITOR not provided
Variation info
Gene KLF1
CLNDBN BLOOD GROUP--LUTHERAN INHIBITOR not provided
Reversed 1
HGVS NC_000019.9:g.12996149G>A; NC_000019.9:g.12996149G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000009565.2, RCV000087158.1,