rs794726687

Merged into

rs528069912

Orientation

plus

Stabilized

plus

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

Make rs794726687(-;-)

Make rs794726687(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

108898939

Gene

GPSM2

is a	snp
is	mentioned by
dbSNP	rs794726687
dbSNP (classic)	rs794726687
ClinGen	rs794726687
ebi	rs794726687
HLI	rs794726687
Exac	rs794726687
Gnomad	rs794726687
Varsome	rs794726687
LitVar	rs794726687
Map	rs794726687
PheGenI	rs794726687
Biobank	rs794726687
1000 genomes	rs794726687
hgdp	rs794726687
ensembl	rs794726687
geneview	rs794726687
scholar	rs794726687
google	rs794726687
pharmgkb	rs794726687
gwascentral	rs794726687
openSNP	rs794726687
23andMe	rs794726687
SNPshot	rs794726687
SNPdbe	rs794726687
MSV3d	rs794726687
GWAS Ctlg	rs794726687

Status

Merged into rs528069912

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs794726687(C;C)
Significance	Pathogenic
Disease	Chudley-McCullough syndrome not provided
Variation	info
Gene	GPSM2
CLNDBN	Chudley-McCullough syndrome not provided
Reversed	0
HGVS	NC_000001.10:g.109441561delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000029164.4, RCV000223985.1,