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rs397514687

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514687(C;T)
Make rs397514687(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position148741411
GeneAGTR1
is asnp
is mentioned by
dbSNPrs397514687
ebirs397514687
HLIrs397514687
Exacrs397514687
Varsomers397514687
Maprs397514687
PheGenIrs397514687
hapmaprs397514687
1000 genomesrs397514687
hgdprs397514687
ensemblrs397514687
gopubmedrs397514687
geneviewrs397514687
scholarrs397514687
googlers397514687
pharmgkbrs397514687
gwascentralrs397514687
openSNPrs397514687
23andMers397514687
23andMe allrs397514687
SNP Nexus

SNPshotrs397514687
SNPdbers397514687
MSV3drs397514687
GWAS Ctlgrs397514687
Max Magnitude0
ClinVar
Risk rs397514687(T;T)
Alt rs397514687(T;T)
Reference rs397514687(C;C)
Significance Pathogenic
Disease Renal dysplasia
Variation info
Gene AGTR1
CLNDBN Renal dysplasia
Reversed 0
HGVS NC_000003.11:g.148459198C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000043469.25,