rs878853316

Orientation

minus

Stabilized

minus

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

Make rs878853316(C;T)

Make rs878853316(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

155239663

Gene

GBA

is a	snp
is	mentioned by
dbSNP	rs878853316
dbSNP (classic)	rs878853316
ClinGen	rs878853316
ebi	rs878853316
HLI	rs878853316
Exac	rs878853316
Gnomad	rs878853316
Varsome	rs878853316
LitVar	rs878853316
Map	rs878853316
PheGenI	rs878853316
Biobank	rs878853316
1000 genomes	rs878853316
hgdp	rs878853316
ensembl	rs878853316
geneview	rs878853316
scholar	rs878853316
google	rs878853316
pharmgkb	rs878853316
gwascentral	rs878853316
openSNP	rs878853316
23andMe	rs878853316
SNPshot	rs878853316
SNPdbe	rs878853316
MSV3d	rs878853316
GWAS Ctlg	rs878853316

Max Magnitude

0

ClinVar
Risk	rs878853316(T;T)
Alt	rs878853316(T;T)
Reference	Rs878853316(C;C)
Significance	Probable-Pathogenic
Disease	Gaucher's disease
Variation	info
Gene	GBA
CLNDBN	Gaucher's disease, type 1
Reversed	1
HGVS	NC_000001.10:g.155209454G>A
CLNSRC
CLNACC	RCV000225500.1,