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rs387906577

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs387906577(-;T)
Make rs387906577(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position148741145
GeneAGTR1
is asnp
is mentioned by
dbSNPrs387906577
dbSNP (old)rs387906577
ClinGenrs387906577
ebirs387906577
HLIrs387906577
Exacrs387906577
Varsomers387906577
Maprs387906577
PheGenIrs387906577
Biobankrs387906577
1000 genomesrs387906577
hgdprs387906577
ensemblrs387906577
gopubmedrs387906577
geneviewrs387906577
scholarrs387906577
googlers387906577
pharmgkbrs387906577
gwascentralrs387906577
openSNPrs387906577
23andMers387906577
23andMe allrs387906577
SNP Nexus

SNPshotrs387906577
SNPdbers387906577
MSV3drs387906577
GWAS Ctlgrs387906577
Max Magnitude0
ClinVar
Risk rs387906577(T;T)
Alt rs387906577(T;T)
Reference Rs387906577(-;-)
Significance Pathogenic
Disease Renal dysplasia
Variation info
Gene AGTR1
CLNDBN Renal dysplasia
Reversed 0
HGVS NC_000003.11:g.148458932dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000019689.30,