rs761396172

Orientation

plus

Stabilized

plus

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

Make rs761396172(C;C)

Make rs761396172(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

165765058

Gene

GALNT3

is a	snp
is	mentioned by
dbSNP	rs761396172
dbSNP (classic)	rs761396172
ClinGen	rs761396172
ebi	rs761396172
HLI	rs761396172
Exac	rs761396172
Gnomad	rs761396172
Varsome	rs761396172
LitVar	rs761396172
Map	rs761396172
PheGenI	rs761396172
Biobank	rs761396172
1000 genomes	rs761396172
hgdp	rs761396172
ensembl	rs761396172
geneview	rs761396172
scholar	rs761396172
google	rs761396172
pharmgkb	rs761396172
gwascentral	rs761396172
openSNP	rs761396172
23andMe	rs761396172
SNPshot	rs761396172
SNPdbe	rs761396172
MSV3d	rs761396172
GWAS Ctlg	rs761396172

Max Magnitude

0

ClinVar
Risk	rs761396172(A;A) rs761396172(C;C)
Alt	rs761396172(A;A) rs761396172(C;C)
Reference	Rs761396172(T;T)
Significance	Pathogenic
Disease	Tumoral calcinosis
Variation	info
Gene	GALNT3
CLNDBN	Tumoral calcinosis, familial, hyperphosphatemic
Reversed	0
HGVS	NC_000002.11:g.166621568T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008237.4,