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rs104893677

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893677(C;T)
Make rs104893677(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position148741880
GeneAGTR1
is asnp
is mentioned by
dbSNPrs104893677
ebirs104893677
HLIrs104893677
Exacrs104893677
Varsomers104893677
Maprs104893677
PheGenIrs104893677
hapmaprs104893677
1000 genomesrs104893677
hgdprs104893677
ensemblrs104893677
gopubmedrs104893677
geneviewrs104893677
scholarrs104893677
googlers104893677
pharmgkbrs104893677
gwascentralrs104893677
openSNPrs104893677
23andMers104893677
23andMe allrs104893677
SNP Nexus

SNPshotrs104893677
SNPdbers104893677
MSV3drs104893677
GWAS Ctlgrs104893677
Max Magnitude0
OMIM106165
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104893677(T;T)
Alt rs104893677(T;T)
Reference rs104893677(C;C)
Significance Pathogenic
Disease Renal dysplasia
Variation info
Gene AGTR1
CLNDBN Renal dysplasia
Reversed 0
HGVS NC_000003.11:g.148459667C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019690.27,