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rs121918132

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918132(C;T)
Make rs121918132(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position44813527
GeneBCAM
is asnp
is mentioned by
dbSNPrs121918132
ebirs121918132
HLIrs121918132
Exacrs121918132
Varsomers121918132
Maprs121918132
PheGenIrs121918132
hapmaprs121918132
1000 genomesrs121918132
hgdprs121918132
ensemblrs121918132
gopubmedrs121918132
geneviewrs121918132
scholarrs121918132
googlers121918132
pharmgkbrs121918132
gwascentralrs121918132
openSNPrs121918132
23andMers121918132
23andMe allrs121918132
SNP Nexus

SNPshotrs121918132
SNPdbers121918132
MSV3drs121918132
GWAS Ctlgrs121918132
Max Magnitude0
OMIM612773
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121918132(T;T)
Alt rs121918132(T;T)
Reference rs121918132(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.45316784C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000469.2,