rs367682612

Orientation

plus

Stabilized

plus

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

Make rs367682612(C;T)

Make rs367682612(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

108904155

Gene

GPSM2

is a	snp
is	mentioned by
dbSNP	rs367682612
dbSNP (classic)	rs367682612
ClinGen	rs367682612
ebi	rs367682612
HLI	rs367682612
Exac	rs367682612
Gnomad	rs367682612
Varsome	rs367682612
LitVar	rs367682612
Map	rs367682612
PheGenI	rs367682612
Biobank	rs367682612
1000 genomes	rs367682612
hgdp	rs367682612
ensembl	rs367682612
geneview	rs367682612
scholar	rs367682612
google	rs367682612
pharmgkb	rs367682612
gwascentral	rs367682612
openSNP	rs367682612
23andMe	rs367682612
SNPshot	rs367682612
SNPdbe	rs367682612
MSV3d	rs367682612
GWAS Ctlg	rs367682612

Max Magnitude

0

ClinVar
Risk	rs367682612(T;T)
Alt	rs367682612(T;T)
Reference	Rs367682612(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GPSM2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.109446777C>T
CLNSRC
CLNACC	RCV000483353.1,