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rs398122935

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122935(A;A)
Make rs398122935(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position148741286
GeneAGTR1
is asnp
is mentioned by
dbSNPrs398122935
ebirs398122935
HLIrs398122935
Exacrs398122935
Varsomers398122935
Maprs398122935
PheGenIrs398122935
hapmaprs398122935
1000 genomesrs398122935
hgdprs398122935
ensemblrs398122935
gopubmedrs398122935
geneviewrs398122935
scholarrs398122935
googlers398122935
pharmgkbrs398122935
gwascentralrs398122935
openSNPrs398122935
23andMers398122935
23andMe allrs398122935
SNP Nexus

SNPshotrs398122935
SNPdbers398122935
MSV3drs398122935
GWAS Ctlgrs398122935
Max Magnitude0
ClinVar
Risk rs398122935(A;A)
Alt rs398122935(A;A)
Reference rs398122935(G;G)
Significance Pathogenic
Disease Renal dysplasia
Variation info
Gene AGTR1
CLNDBN Renal dysplasia
Reversed 0
HGVS NC_000003.11:g.148459073G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000043468.25,