rs869025582

Orientation

plus

Stabilized

plus

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

Make rs869025582(G;T)

Make rs869025582(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

151287016

Gene

ZNF687

is a	snp
is	mentioned by
dbSNP	rs869025582
dbSNP (classic)	rs869025582
ClinGen	rs869025582
ebi	rs869025582
HLI	rs869025582
Exac	rs869025582
Gnomad	rs869025582
Varsome	rs869025582
LitVar	rs869025582
Map	rs869025582
PheGenI	rs869025582
Biobank	rs869025582
1000 genomes	rs869025582
hgdp	rs869025582
ensembl	rs869025582
geneview	rs869025582
scholar	rs869025582
google	rs869025582
pharmgkb	rs869025582
gwascentral	rs869025582
openSNP	rs869025582
23andMe	rs869025582
SNPshot	rs869025582
SNPdbe	rs869025582
MSV3d	rs869025582
GWAS Ctlg	rs869025582

Max Magnitude

0

ClinVar
Risk	rs869025582(T;T)
Alt	rs869025582(T;T)
Reference	Rs869025582(G;G)
Significance	Pathogenic
Disease	Paget disease of bone 6
Variation	info
Gene	ZNF687
CLNDBN	Paget disease of bone 6
Reversed	0
HGVS	NC_000001.10:g.151259492G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000208590.1,