rs772372530

Orientation

plus

Stabilized

plus

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

Make rs772372530(-;-)

Make rs772372530(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

108922447

Gene

GPSM2

is a	snp
is	mentioned by
dbSNP	rs772372530
dbSNP (classic)	rs772372530
ClinGen	rs772372530
ebi	rs772372530
HLI	rs772372530
Exac	rs772372530
Gnomad	rs772372530
Varsome	rs772372530
LitVar	rs772372530
Map	rs772372530
PheGenI	rs772372530
Biobank	rs772372530
1000 genomes	rs772372530
hgdp	rs772372530
ensembl	rs772372530
geneview	rs772372530
scholar	rs772372530
google	rs772372530
pharmgkb	rs772372530
gwascentral	rs772372530
openSNP	rs772372530
23andMe	rs772372530
SNPshot	rs772372530
SNPdbe	rs772372530
MSV3d	rs772372530
GWAS Ctlg	rs772372530

Merged from

Rs886045026

Max Magnitude

0

ClinVar
Risk	rs772372530(-;-)
Alt	rs772372530(-;-)
Reference	Rs772372530(G;G)
Significance	Pathogenic
Disease	not provided GPSM2-Related Disorders
Variation	info
Gene	GPSM2
CLNDBN	not provided GPSM2-Related Disorders
Reversed	0
HGVS	NC_000001.10:g.109465071delG
CLNSRC
CLNACC	RCV000224236.1, RCV000380707.1,