Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777684

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777684(C;T)
Make rs587777684(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position32081419
GeneTNXB
is asnp
is mentioned by
dbSNPrs587777684
ebirs587777684
HLIrs587777684
Exacrs587777684
Varsomers587777684
Maprs587777684
PheGenIrs587777684
hapmaprs587777684
1000 genomesrs587777684
hgdprs587777684
ensemblrs587777684
gopubmedrs587777684
geneviewrs587777684
scholarrs587777684
googlers587777684
pharmgkbrs587777684
gwascentralrs587777684
openSNPrs587777684
23andMers587777684
23andMe allrs587777684
SNP Nexus

SNPshotrs587777684
SNPdbers587777684
MSV3drs587777684
GWAS Ctlgrs587777684
Max Magnitude0
ClinVar
Risk rs587777684(C,T;C,T)
Alt rs587777684(C,T;C,T)
Reference rs587777684(G;G)
Significance Pathogenic
Disease Vesicoureteral reflux 8
Variation info
Gene TNXB
CLNDBN Vesicoureteral reflux 8
Reversed 1
HGVS NC_000006.11:g.32049196C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000133611.3,