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rs121918586

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918586(A;A)
Make rs121918586(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position49619284
GeneRHAG
is asnp
is mentioned by
dbSNPrs121918586
ebirs121918586
HLIrs121918586
Exacrs121918586
Varsomers121918586
Maprs121918586
PheGenIrs121918586
hapmaprs121918586
1000 genomesrs121918586
hgdprs121918586
ensemblrs121918586
gopubmedrs121918586
geneviewrs121918586
scholarrs121918586
googlers121918586
pharmgkbrs121918586
gwascentralrs121918586
openSNPrs121918586
23andMers121918586
23andMe allrs121918586
SNP Nexus

SNPshotrs121918586
SNPdbers121918586
MSV3drs121918586
GWAS Ctlgrs121918586
Max Magnitude0
OMIM180297
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121918586(A,C;A,C)
Alt rs121918586(A,C;A,C)
Reference rs121918586(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.49586997C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013934.23,