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rs121917742

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917742(A;A)
Make rs121917742(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position204159399
GeneREN
is asnp
is mentioned by
dbSNPrs121917742
ebirs121917742
HLIrs121917742
Exacrs121917742
Varsomers121917742
Maprs121917742
PheGenIrs121917742
hapmaprs121917742
1000 genomesrs121917742
hgdprs121917742
ensemblrs121917742
gopubmedrs121917742
geneviewrs121917742
scholarrs121917742
googlers121917742
pharmgkbrs121917742
gwascentralrs121917742
openSNPrs121917742
23andMers121917742
23andMe allrs121917742
SNP Nexus

SNPshotrs121917742
SNPdbers121917742
MSV3drs121917742
GWAS Ctlgrs121917742
Max Magnitude0
OMIM179820
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121917742(A;A)
Alt rs121917742(A;A)
Reference rs121917742(G;G)
Significance Pathogenic
Disease Renal dysplasia
Variation info
Gene REN
CLNDBN Renal dysplasia
Reversed 1
HGVS NC_000001.10:g.204128527C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014004.17,