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rs121918133

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918133(C;T)
Make rs121918133(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position44812319
GeneBCAM
is asnp
is mentioned by
dbSNPrs121918133
ebirs121918133
HLIrs121918133
Exacrs121918133
Varsomers121918133
Maprs121918133
PheGenIrs121918133
hapmaprs121918133
1000 genomesrs121918133
hgdprs121918133
ensemblrs121918133
gopubmedrs121918133
geneviewrs121918133
scholarrs121918133
googlers121918133
pharmgkbrs121918133
gwascentralrs121918133
openSNPrs121918133
23andMers121918133
23andMe allrs121918133
SNP Nexus

SNPshotrs121918133
SNPdbers121918133
MSV3drs121918133
GWAS Ctlgrs121918133
Max Magnitude0
OMIM612773
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121918133(T;T)
Alt rs121918133(T;T)
Reference rs121918133(C;C)
Significance Pathogenic
Disease BLOOD GROUP--LUTHERAN NULL
Variation info
Gene BCAM
CLNDBN BLOOD GROUP--LUTHERAN NULL
Reversed 0
HGVS NC_000019.9:g.45315576C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000472.1,