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rs56001514

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs56001514(C;T)
Make rs56001514(T;T)
ReferenceGRCh38 38.1/142
Chromosome15
Position74411926
GeneSEMA7A
is asnp
is mentioned by
dbSNPrs56001514
ebirs56001514
HLIrs56001514
Exacrs56001514
Varsomers56001514
Maprs56001514
PheGenIrs56001514
hapmaprs56001514
1000 genomesrs56001514
hgdprs56001514
ensemblrs56001514
gopubmedrs56001514
geneviewrs56001514
scholarrs56001514
googlers56001514
pharmgkbrs56001514
gwascentralrs56001514
openSNPrs56001514
23andMers56001514
23andMe allrs56001514
SNP Nexus

SNPshotrs56001514
SNPdbers56001514
MSV3drs56001514
GWAS Ctlgrs56001514
Max Magnitude0
ClinVar
Risk rs56001514(T;T)
Alt rs56001514(T;T)
Reference rs56001514(C;C)
Significance Other
Disease John Milton Hagen blood group system
Variation info
Gene MIR6881 SEMA7A
CLNDBN John Milton Hagen blood group system
Reversed 1
HGVS NC_000015.9:g.74704267G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000029235.3,