rs137853089

Orientation

minus

Stabilized

minus

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

Make rs137853089(C;T)

Make rs137853089(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

165755015

Gene

GALNT3

is a	snp
is	mentioned by
dbSNP	rs137853089
dbSNP (classic)	rs137853089
ClinGen	rs137853089
ebi	rs137853089
HLI	rs137853089
Exac	rs137853089
Gnomad	rs137853089
Varsome	rs137853089
LitVar	rs137853089
Map	rs137853089
PheGenI	rs137853089
Biobank	rs137853089
1000 genomes	rs137853089
hgdp	rs137853089
ensembl	rs137853089
geneview	rs137853089
scholar	rs137853089
google	rs137853089
pharmgkb	rs137853089
gwascentral	rs137853089
openSNP	rs137853089
23andMe	rs137853089
SNPshot	rs137853089
SNPdbe	rs137853089
MSV3d	rs137853089
GWAS Ctlg	rs137853089

Max Magnitude

0

OMIM	601756
Desc
Variant	0007
Related	also

ClinVar
Risk	rs137853089(T;T)
Alt	rs137853089(T;T)
Reference	Rs137853089(C;C)
Significance	Pathogenic
Disease	Tumoral calcinosis
Variation	info
Gene	GALNT3
CLNDBN	Tumoral calcinosis, familial, hyperphosphatemic
Reversed	1
HGVS	NC_000002.11:g.166611525G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008241.3,