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rs397514691

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514691(A;A)
Make rs397514691(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position204160648
GeneREN
is asnp
is mentioned by
dbSNPrs397514691
ebirs397514691
HLIrs397514691
Exacrs397514691
Varsomers397514691
Maprs397514691
PheGenIrs397514691
hapmaprs397514691
1000 genomesrs397514691
hgdprs397514691
ensemblrs397514691
gopubmedrs397514691
geneviewrs397514691
scholarrs397514691
googlers397514691
pharmgkbrs397514691
gwascentralrs397514691
openSNPrs397514691
23andMers397514691
23andMe allrs397514691
SNP Nexus

SNPshotrs397514691
SNPdbers397514691
MSV3drs397514691
GWAS Ctlgrs397514691
Max Magnitude0
ClinVar
Risk rs397514691(A;A)
Alt rs397514691(A;A)
Reference rs397514691(C;C)
Significance Pathogenic
Disease Renal dysplasia
Variation info
Gene REN
CLNDBN Renal dysplasia
Reversed 1
HGVS NC_000001.10:g.204129776G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000043473.24,