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rs267607082

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607082(G;T)
Make rs267607082(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position54459282
GeneSOX17
is asnp
is mentioned by
dbSNPrs267607082
ebirs267607082
HLIrs267607082
Exacrs267607082
Varsomers267607082
Maprs267607082
PheGenIrs267607082
hapmaprs267607082
1000 genomesrs267607082
hgdprs267607082
ensemblrs267607082
gopubmedrs267607082
geneviewrs267607082
scholarrs267607082
googlers267607082
pharmgkbrs267607082
gwascentralrs267607082
openSNPrs267607082
23andMers267607082
23andMe allrs267607082
SNP Nexus

SNPshotrs267607082
SNPdbers267607082
MSV3drs267607082
GWAS Ctlgrs267607082
Max Magnitude0
ClinVar
Risk rs267607082(A,C,T;A,C,T)
Alt rs267607082(A,C,T;A,C,T)
Reference rs267607082(G;G)
Significance Pathogenic
Disease Vesicoureteral reflux 3
Variation info
Gene SOX17
CLNDBN Vesicoureteral reflux 3
Reversed 0
HGVS NC_000008.10:g.55371842G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001141.2,