rs797044776

Orientation

minus

Stabilized

minus

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

Make rs797044776(C;T)

Make rs797044776(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

101398012

Gene	GLA, RPL36A-HNRNPH2

is a	snp
is	mentioned by
dbSNP	rs797044776
dbSNP (classic)	rs797044776
ClinGen	rs797044776
ebi	rs797044776
HLI	rs797044776
Exac	rs797044776
Gnomad	rs797044776
Varsome	rs797044776
LitVar	rs797044776
Map	rs797044776
PheGenI	rs797044776
Biobank	rs797044776
1000 genomes	rs797044776
hgdp	rs797044776
ensembl	rs797044776
geneview	rs797044776
scholar	rs797044776
google	rs797044776
pharmgkb	rs797044776
gwascentral	rs797044776
openSNP	rs797044776
23andMe	rs797044776
SNPshot	rs797044776
SNPdbe	rs797044776
MSV3d	rs797044776
GWAS Ctlg	rs797044776

Max Magnitude

0

ClinVar
Risk	rs797044776(T;T)
Alt	rs797044776(T;T)
Reference	Rs797044776(C;C)
Significance	Pathogenic
Disease	Fabry disease
Variation	info
Gene	RPL36A-HNRNPH2 GLA
CLNDBN	Fabry disease
Reversed	1
HGVS	NC_000023.10:g.100653000G>A
CLNSRC
CLNACC	RCV000179729.1,