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rs267607083

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607083(A;A)
Make rs267607083(A;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position54459525
GeneSOX17
is asnp
is mentioned by
dbSNPrs267607083
ebirs267607083
HLIrs267607083
Exacrs267607083
Varsomers267607083
Maprs267607083
PheGenIrs267607083
hapmaprs267607083
1000 genomesrs267607083
hgdprs267607083
ensemblrs267607083
gopubmedrs267607083
geneviewrs267607083
scholarrs267607083
googlers267607083
pharmgkbrs267607083
gwascentralrs267607083
openSNPrs267607083
23andMers267607083
23andMe allrs267607083
SNP Nexus

SNPshotrs267607083
SNPdbers267607083
MSV3drs267607083
GWAS Ctlgrs267607083
Max Magnitude0
ClinVar
Risk rs267607083(A;A)
Alt rs267607083(A;A)
Reference rs267607083(T;T)
Significance Pathogenic
Disease Vesicoureteral reflux 3
Variation info
Gene SOX17
CLNDBN Vesicoureteral reflux 3
Reversed 0
HGVS NC_000008.10:g.55372085T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001140.2,