rs761634625

Orientation

plus

Stabilized

plus

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

Make rs761634625(-;-)

Make rs761634625(-;GCT)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

25737357

Gene

NGLY1

is a	snp
is	mentioned by
dbSNP	rs761634625
dbSNP (classic)	rs761634625
ClinGen	rs761634625
ebi	rs761634625
HLI	rs761634625
Exac	rs761634625
Gnomad	rs761634625
Varsome	rs761634625
LitVar	rs761634625
Map	rs761634625
PheGenI	rs761634625
Biobank	rs761634625
1000 genomes	rs761634625
hgdp	rs761634625
ensembl	rs761634625
geneview	rs761634625
scholar	rs761634625
google	rs761634625
pharmgkb	rs761634625
gwascentral	rs761634625
openSNP	rs761634625
23andMe	rs761634625
SNPshot	rs761634625
SNPdbe	rs761634625
MSV3d	rs761634625
GWAS Ctlg	rs761634625

Max Magnitude

0

ClinVar
Risk	rs761634625(-;-)
Alt	rs761634625(-;-)
Reference	Rs761634625(GCT;GCT)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NGLY1
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.25778848_25778850delGCT
CLNSRC
CLNACC	RCV000483669.1,