rs587777684

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(G;G)	0	common in clinvar

Make rs587777684(C;T)

Make rs587777684(T;T)

Reference

GRCh38 38.1/142

Chromosome

6

Position

32081419

Gene

TNXB

is a	snp
is	mentioned by
dbSNP	rs587777684
dbSNP (classic)	rs587777684
ClinGen	rs587777684
ebi	rs587777684
HLI	rs587777684
Exac	rs587777684
Gnomad	rs587777684
Varsome	rs587777684
LitVar	rs587777684
Map	rs587777684
PheGenI	rs587777684
Biobank	rs587777684
1000 genomes	rs587777684
hgdp	rs587777684
ensembl	rs587777684
geneview	rs587777684
scholar	rs587777684
google	rs587777684
pharmgkb	rs587777684
gwascentral	rs587777684
openSNP	rs587777684
23andMe	rs587777684
SNPshot	rs587777684
SNPdbe	rs587777684
MSV3d	rs587777684
GWAS Ctlg	rs587777684

Max Magnitude

0

ClinVar
Risk	Rs587777684(C;C) rs587777684(T;T)
Alt	Rs587777684(C;C) rs587777684(T;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,