rs886045026

Merged into

rs772372530

Orientation

plus

Stabilized

plus

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

is a	snp
is	mentioned by
dbSNP	rs886045026
dbSNP (classic)	rs886045026
ClinGen	rs886045026
ebi	rs886045026
HLI	rs886045026
Exac	rs886045026
Gnomad	rs886045026
Varsome	rs886045026
LitVar	rs886045026
Map	rs886045026
PheGenI	rs886045026
Biobank	rs886045026
1000 genomes	rs886045026
hgdp	rs886045026
ensembl	rs886045026
geneview	rs886045026
scholar	rs886045026
google	rs886045026
pharmgkb	rs886045026
gwascentral	rs886045026
openSNP	rs886045026
23andMe	rs886045026
SNPshot	rs886045026
SNPdbe	rs886045026
MSV3d	rs886045026
GWAS Ctlg	rs886045026

Status

Merged into rs772372530

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs886045026(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	Illumina
CLNACC	RCV000224236.1, RCV000380707.1,