rs777695770

Orientation

plus

Stabilized

plus

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

Make rs777695770(G;T)

Make rs777695770(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

108903235

Gene

GPSM2

is a	snp
is	mentioned by
dbSNP	rs777695770
dbSNP (classic)	rs777695770
ClinGen	rs777695770
ebi	rs777695770
HLI	rs777695770
Exac	rs777695770
Gnomad	rs777695770
Varsome	rs777695770
LitVar	rs777695770
Map	rs777695770
PheGenI	rs777695770
Biobank	rs777695770
1000 genomes	rs777695770
hgdp	rs777695770
ensembl	rs777695770
geneview	rs777695770
scholar	rs777695770
google	rs777695770
pharmgkb	rs777695770
gwascentral	rs777695770
openSNP	rs777695770
23andMe	rs777695770
SNPshot	rs777695770
SNPdbe	rs777695770
MSV3d	rs777695770
GWAS Ctlg	rs777695770

Max Magnitude

0

ClinVar
Risk	rs777695770(T;T)
Alt	rs777695770(T;T)
Reference	Rs777695770(G;G)
Significance	Pathogenic
Disease	Chudley-McCullough syndrome
Variation	info
Gene	GPSM2
CLNDBN	Chudley-McCullough syndrome
Reversed	0
HGVS	NC_000001.10:g.109445857G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000029166.5,