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

rs587777683

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777683(A;A)
Make rs587777683(A;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position32048638
GeneTNXB
is asnp
is mentioned by
dbSNPrs587777683
ebirs587777683
HLIrs587777683
Exacrs587777683
Varsomers587777683
Maprs587777683
PheGenIrs587777683
hapmaprs587777683
1000 genomesrs587777683
hgdprs587777683
ensemblrs587777683
gopubmedrs587777683
geneviewrs587777683
scholarrs587777683
googlers587777683
pharmgkbrs587777683
gwascentralrs587777683
openSNPrs587777683
23andMers587777683
23andMe allrs587777683
SNP Nexus

SNPshotrs587777683
SNPdbers587777683
MSV3drs587777683
GWAS Ctlgrs587777683
Max Magnitude0
ClinVar
Risk rs587777683(A;A)
Alt rs587777683(A;A)
Reference rs587777683(G;G)
Significance Pathogenic
Disease Vesicoureteral reflux 8
Variation info
Gene TNXB
CLNDBN Vesicoureteral reflux 8
Reversed 0
HGVS NC_000006.11:g.32016415G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000133610.2,