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rs104894669

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894669(A;A)
Make rs104894669(A;G)
ReferenceGRCh37 37.1/132
Chromosome19
Position580428
GeneBSG
is asnp
is mentioned by
dbSNPrs104894669
ebirs104894669
HLIrs104894669
Exacrs104894669
Varsomers104894669
Maprs104894669
PheGenIrs104894669
hapmaprs104894669
1000 genomesrs104894669
hgdprs104894669
ensemblrs104894669
gopubmedrs104894669
geneviewrs104894669
scholarrs104894669
googlers104894669
pharmgkbrs104894669
gwascentralrs104894669
openSNPrs104894669
23andMers104894669
23andMe allrs104894669
SNP Nexus

SNPshotrs104894669
SNPdbers104894669
MSV3drs104894669
GWAS Ctlgrs104894669
Max Magnitude0
OMIM109480
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894669(A;A)
Alt rs104894669(A;A)
Reference rs104894669(G;G)
Significance Other
Disease BLOOD GROUP--OK
Variation info
Gene BSG
CLNDBN BLOOD GROUP--OK
Reversed 0
HGVS NC_000019.9:g.580428G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019327.24,