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rs121917831

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917831(C;G)
Make rs121917831(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position11378233
GeneEPOR
is asnp
is mentioned by
dbSNPrs121917831
ebirs121917831
HLIrs121917831
Exacrs121917831
Varsomers121917831
Maprs121917831
PheGenIrs121917831
hapmaprs121917831
1000 genomesrs121917831
hgdprs121917831
ensemblrs121917831
gopubmedrs121917831
geneviewrs121917831
scholarrs121917831
googlers121917831
pharmgkbrs121917831
gwascentralrs121917831
openSNPrs121917831
23andMers121917831
23andMe allrs121917831
SNP Nexus

SNPshotrs121917831
SNPdbers121917831
MSV3drs121917831
GWAS Ctlgrs121917831
Max Magnitude0
ClinVar
Risk rs121917831(G,T;G,T)
Alt rs121917831(G,T;G,T)
Reference rs121917831(C;C)
Significance Other
Disease Familial erythrocytosis
Variation info
Gene EPOR
CLNDBN Familial erythrocytosis, 1
Reversed 1
HGVS NC_000019.9:g.11488909G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000018071.28,