rs727503119

Orientation

minus

Stabilized

minus

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

Make rs727503119(G;T)

Make rs727503119(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

120446304

Gene

LAMP2

is a	snp
is	mentioned by
dbSNP	rs727503119
dbSNP (classic)	rs727503119
ClinGen	rs727503119
ebi	rs727503119
HLI	rs727503119
Exac	rs727503119
Gnomad	rs727503119
Varsome	rs727503119
LitVar	rs727503119
Map	rs727503119
PheGenI	rs727503119
Biobank	rs727503119
1000 genomes	rs727503119
hgdp	rs727503119
ensembl	rs727503119
geneview	rs727503119
scholar	rs727503119
google	rs727503119
pharmgkb	rs727503119
gwascentral	rs727503119
openSNP	rs727503119
23andMe	rs727503119
SNPshot	rs727503119
SNPdbe	rs727503119
MSV3d	rs727503119
GWAS Ctlg	rs727503119

Max Magnitude

0

ClinVar
Risk	rs727503119(A;A) rs727503119(T;T)
Alt	rs727503119(A;A) rs727503119(T;T)
Reference	Rs727503119(G;G)
Significance	Pathogenic
Disease	Danon disease not provided
Variation	info
Gene	LAMP2
CLNDBN	Danon disease not provided
Reversed	1
HGVS	NC_000023.10:g.119580159C>A; NC_000023.10:g.119580159C>T
CLNSRC
CLNACC	RCV000150912.1, RCV000157972.1, RCV000157971.1,