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rs387907241

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907241(G;T)
Make rs387907241(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position74414893
GeneSEMA7A
is asnp
is mentioned by
dbSNPrs387907241
ebirs387907241
HLIrs387907241
Exacrs387907241
Varsomers387907241
Maprs387907241
PheGenIrs387907241
hapmaprs387907241
1000 genomesrs387907241
hgdprs387907241
ensemblrs387907241
gopubmedrs387907241
geneviewrs387907241
scholarrs387907241
googlers387907241
pharmgkbrs387907241
gwascentralrs387907241
openSNPrs387907241
23andMers387907241
23andMe allrs387907241
SNP Nexus

SNPshotrs387907241
SNPdbers387907241
MSV3drs387907241
GWAS Ctlgrs387907241
Max Magnitude0
ClinVar
Risk rs387907241(T;T)
Alt rs387907241(T;T)
Reference rs387907241(G;G)
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.74707234C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000029236.3,