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rs121917741

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917741(C;T)
Make rs121917741(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position204162117
GeneREN
is asnp
is mentioned by
dbSNPrs121917741
ClinGenrs121917741
ebirs121917741
HLIrs121917741
Exacrs121917741
Varsomers121917741
Maprs121917741
PheGenIrs121917741
hapmaprs121917741
1000 genomesrs121917741
hgdprs121917741
ensemblrs121917741
gopubmedrs121917741
geneviewrs121917741
scholarrs121917741
googlers121917741
pharmgkbrs121917741
gwascentralrs121917741
openSNPrs121917741
23andMers121917741
23andMe allrs121917741
SNP Nexus

SNPshotrs121917741
SNPdbers121917741
MSV3drs121917741
GWAS Ctlgrs121917741
Max Magnitude0
OMIM179820
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121917741(T;T)
Alt rs121917741(T;T)
Reference Rs121917741(C;C)
Significance Pathogenic
Disease Renal dysplasia
Variation info
Gene REN
CLNDBN Renal dysplasia
Reversed 1
HGVS NC_000001.10:g.204131245G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014003.17,