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rs3810141

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3810141(A;A)
Make rs3810141(A;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position44813547
GeneBCAM
is asnp
is mentioned by
dbSNPrs3810141
ebirs3810141
HLIrs3810141
Exacrs3810141
Varsomers3810141
Maprs3810141
PheGenIrs3810141
hapmaprs3810141
1000 genomesrs3810141
hgdprs3810141
ensemblrs3810141
gopubmedrs3810141
geneviewrs3810141
scholarrs3810141
googlers3810141
pharmgkbrs3810141
gwascentralrs3810141
openSNPrs3810141
23andMers3810141
23andMe allrs3810141
SNP Nexus

SNPshotrs3810141
SNPdbers3810141
MSV3drs3810141
GWAS Ctlgrs3810141
GMAF0.05785
Max Magnitude0
OMIM612773
Desc
Variant0005
Relatedalso
ClinVar
Risk rs3810141(A;A)
Alt rs3810141(A;A)
Reference rs3810141(G;G)
Significance Pathogenic
Disease BLOOD GROUP--LUTHERAN NULL
Variation info
Gene BCAM
CLNDBN BLOOD GROUP--LUTHERAN NULL
Reversed 1
HGVS NC_000019.9:g.45316804C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000471.2,