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rs56136737

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs56136737(C;G)
Make rs56136737(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position42830860
GeneERMAP
is asnp
is mentioned by
dbSNPrs56136737
ebirs56136737
HLIrs56136737
Exacrs56136737
Varsomers56136737
Maprs56136737
PheGenIrs56136737
hapmaprs56136737
1000 genomesrs56136737
hgdprs56136737
ensemblrs56136737
gopubmedrs56136737
geneviewrs56136737
scholarrs56136737
googlers56136737
pharmgkbrs56136737
gwascentralrs56136737
openSNPrs56136737
23andMers56136737
23andMe allrs56136737
SNP Nexus

SNPshotrs56136737
SNPdbers56136737
MSV3drs56136737
GWAS Ctlgrs56136737
Max Magnitude0
OMIM609017
Desc
Variant0003
Relatedalso


ClinVar
Risk rs56136737(G;G)
Alt rs56136737(G;G)
Reference rs56136737(C;C)
Significance Other
Disease Radin blood group
Variation info
Gene ERMAP
CLNDBN Radin blood group
Reversed 0
HGVS NC_000001.10:g.43296531C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001994.3,