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rs121912702

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912702(C;T)
Make rs121912702(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position230710247
GeneAGT
is asnp
is mentioned by
dbSNPrs121912702
ebirs121912702
HLIrs121912702
Exacrs121912702
Varsomers121912702
Maprs121912702
PheGenIrs121912702
hapmaprs121912702
1000 genomesrs121912702
hgdprs121912702
ensemblrs121912702
gopubmedrs121912702
geneviewrs121912702
scholarrs121912702
googlers121912702
pharmgkbrs121912702
gwascentralrs121912702
openSNPrs121912702
23andMers121912702
23andMe allrs121912702
SNP Nexus

SNPshotrs121912702
SNPdbers121912702
MSV3drs121912702
GWAS Ctlgrs121912702
Max Magnitude0
OMIM106150
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121912702(T;T)
Alt rs121912702(T;T)
Reference rs121912702(C;C)
Significance Pathogenic
Disease Renal dysplasia
Variation info
Gene AGT
CLNDBN Renal dysplasia
Reversed 1
HGVS NC_000001.10:g.230845993G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019697.30,