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rs137852687

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852687(A;T)
Make rs137852687(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position12885356
GeneKLF1
is asnp
is mentioned by
dbSNPrs137852687
ebirs137852687
HLIrs137852687
Exacrs137852687
Varsomers137852687
Maprs137852687
PheGenIrs137852687
hapmaprs137852687
1000 genomesrs137852687
hgdprs137852687
ensemblrs137852687
gopubmedrs137852687
geneviewrs137852687
scholarrs137852687
googlers137852687
pharmgkbrs137852687
gwascentralrs137852687
openSNPrs137852687
23andMers137852687
23andMe allrs137852687
SNP Nexus

SNPshotrs137852687
SNPdbers137852687
MSV3drs137852687
GWAS Ctlgrs137852687
Max Magnitude0
OMIM600599
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137852687(G,T;G,T)
Alt rs137852687(G,T;G,T)
Reference rs137852687(A;A)
Significance Pathogenic
Disease BLOOD GROUP--LUTHERAN INHIBITOR
Variation info
Gene KLF1
CLNDBN BLOOD GROUP--LUTHERAN INHIBITOR
Reversed 1
HGVS NC_000019.9:g.12996170T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009564.3,