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rs121918589

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918589(G;T)
Make rs121918589(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position49606921
GeneRHAG
is asnp
is mentioned by
dbSNPrs121918589
ebirs121918589
HLIrs121918589
Exacrs121918589
Varsomers121918589
Maprs121918589
PheGenIrs121918589
hapmaprs121918589
1000 genomesrs121918589
hgdprs121918589
ensemblrs121918589
gopubmedrs121918589
geneviewrs121918589
scholarrs121918589
googlers121918589
pharmgkbrs121918589
gwascentralrs121918589
openSNPrs121918589
23andMers121918589
23andMe allrs121918589
SNP Nexus

SNPshotrs121918589
SNPdbers121918589
MSV3drs121918589
GWAS Ctlgrs121918589
Max Magnitude0
OMIM180297
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121918589(T;T)
Alt rs121918589(T;T)
Reference rs121918589(G;G)
Significance Pathogenic
Disease Rh-null hemolytic anemia
Variation info
Gene RHAG
CLNDBN Rh-null hemolytic anemia, regulator type
Reversed 1
HGVS NC_000006.11:g.49574634C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013941.24,