rs773068151

Orientation

plus

Stabilized

plus

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

Make rs773068151(G;T)

Make rs773068151(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

108904124

Gene

GPSM2

is a	snp
is	mentioned by
dbSNP	rs773068151
dbSNP (classic)	rs773068151
ClinGen	rs773068151
ebi	rs773068151
HLI	rs773068151
Exac	rs773068151
Gnomad	rs773068151
Varsome	rs773068151
LitVar	rs773068151
Map	rs773068151
PheGenI	rs773068151
Biobank	rs773068151
1000 genomes	rs773068151
hgdp	rs773068151
ensembl	rs773068151
geneview	rs773068151
scholar	rs773068151
google	rs773068151
pharmgkb	rs773068151
gwascentral	rs773068151
openSNP	rs773068151
23andMe	rs773068151
SNPshot	rs773068151
SNPdbe	rs773068151
MSV3d	rs773068151
GWAS Ctlg	rs773068151

Max Magnitude

0

ClinVar
Risk	rs773068151(T;T)
Alt	rs773068151(T;T)
Reference	Rs773068151(G;G)
Significance	Pathogenic
Disease	Chudley-McCullough syndrome
Variation	info
Gene	GPSM2
CLNDBN	Chudley-McCullough syndrome
Reversed	0
HGVS	NC_000001.10:g.109446746G>T
CLNSRC
CLNACC	RCV000218080.1,