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rs121918588

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918588(G;T)
Make rs121918588(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position49636810
GeneRHAG
is asnp
is mentioned by
dbSNPrs121918588
ebirs121918588
HLIrs121918588
Exacrs121918588
Varsomers121918588
Maprs121918588
PheGenIrs121918588
hapmaprs121918588
1000 genomesrs121918588
hgdprs121918588
ensemblrs121918588
gopubmedrs121918588
geneviewrs121918588
scholarrs121918588
googlers121918588
pharmgkbrs121918588
gwascentralrs121918588
openSNPrs121918588
23andMers121918588
23andMe allrs121918588
SNP Nexus

SNPshotrs121918588
SNPdbers121918588
MSV3drs121918588
GWAS Ctlgrs121918588
Max Magnitude0
OMIM180297
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121918588(T;T)
Alt rs121918588(T;T)
Reference rs121918588(G;G)
Significance Pathogenic
Disease Rh-mod syndrome
Variation info
Gene RHAG
CLNDBN Rh-mod syndrome
Reversed 1
HGVS NC_000006.11:g.49604523C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013938.24,