rs730880496

Orientation

minus

Stabilized

minus

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

Make rs730880496(C;C)

Make rs730880496(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

120456770

Gene

LAMP2

is a	snp
is	mentioned by
dbSNP	rs730880496
dbSNP (classic)	rs730880496
ClinGen	rs730880496
ebi	rs730880496
HLI	rs730880496
Exac	rs730880496
Gnomad	rs730880496
Varsome	rs730880496
LitVar	rs730880496
Map	rs730880496
PheGenI	rs730880496
Biobank	rs730880496
1000 genomes	rs730880496
hgdp	rs730880496
ensembl	rs730880496
geneview	rs730880496
scholar	rs730880496
google	rs730880496
pharmgkb	rs730880496
gwascentral	rs730880496
openSNP	rs730880496
23andMe	rs730880496
SNPshot	rs730880496
SNPdbe	rs730880496
MSV3d	rs730880496
GWAS Ctlg	rs730880496

Max Magnitude

0

ClinVar
Risk	rs730880496(C;C)
Alt	rs730880496(C;C)
Reference	Rs730880496(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LAMP2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.119590625C>G
CLNSRC
CLNACC	RCV000157989.2,