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rs56204206

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs56204206(A;A)
Make rs56204206(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position74411928
GeneSEMA7A
is asnp
is mentioned by
dbSNPrs56204206
ebirs56204206
HLIrs56204206
Exacrs56204206
Varsomers56204206
Maprs56204206
PheGenIrs56204206
hapmaprs56204206
1000 genomesrs56204206
hgdprs56204206
ensemblrs56204206
gopubmedrs56204206
geneviewrs56204206
scholarrs56204206
googlers56204206
pharmgkbrs56204206
gwascentralrs56204206
openSNPrs56204206
23andMers56204206
23andMe allrs56204206
SNP Nexus

SNPshotrs56204206
SNPdbers56204206
MSV3drs56204206
GWAS Ctlgrs56204206
Max Magnitude0
ClinVar
Risk rs56204206(A;A)
Alt rs56204206(A;A)
Reference rs56204206(G;G)
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.74704269C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000029234.3,