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rs56367230

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs56367230(C;T)
Make rs56367230(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position74417377
GeneSEMA7A
is asnp
is mentioned by
dbSNPrs56367230
ebirs56367230
HLIrs56367230
Exacrs56367230
Varsomers56367230
Maprs56367230
PheGenIrs56367230
hapmaprs56367230
1000 genomesrs56367230
hgdprs56367230
ensemblrs56367230
gopubmedrs56367230
geneviewrs56367230
scholarrs56367230
googlers56367230
pharmgkbrs56367230
gwascentralrs56367230
openSNPrs56367230
23andMers56367230
23andMe allrs56367230
SNP Nexus

SNPshotrs56367230
SNPdbers56367230
MSV3drs56367230
GWAS Ctlgrs56367230
Max Magnitude0
ClinVar
Risk rs56367230(T;T)
Alt rs56367230(T;T)
Reference rs56367230(C;C)
Significance Other
Disease John Milton Hagen blood group system
Variation info
Gene SEMA7A
CLNDBN John Milton Hagen blood group system
Reversed 1
HGVS NC_000015.9:g.74709718G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000029233.3,