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rs55637216

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs55637216(A;A)
Make rs55637216(A;G)
ReferenceGRCh38 38.1/142
Chromosome15
Position74417376
GeneSEMA7A
is asnp
is mentioned by
dbSNPrs55637216
ebirs55637216
HLIrs55637216
Exacrs55637216
Varsomers55637216
Maprs55637216
PheGenIrs55637216
hapmaprs55637216
1000 genomesrs55637216
hgdprs55637216
ensemblrs55637216
gopubmedrs55637216
geneviewrs55637216
scholarrs55637216
googlers55637216
pharmgkbrs55637216
gwascentralrs55637216
openSNPrs55637216
23andMers55637216
23andMe allrs55637216
SNP Nexus

SNPshotrs55637216
SNPdbers55637216
MSV3drs55637216
GWAS Ctlgrs55637216
Max Magnitude0
ClinVar
Risk rs55637216(A;A)
Alt rs55637216(A;A)
Reference rs55637216(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.74709717C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000029232.3,