rs398123208

Orientation

minus

Stabilized

minus

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

Make rs398123208(A;A)

Make rs398123208(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

101403938

Gene	GLA, RPL36A-HNRNPH2

is a	snp
is	mentioned by
dbSNP	rs398123208
dbSNP (classic)	rs398123208
ClinGen	rs398123208
ebi	rs398123208
HLI	rs398123208
Exac	rs398123208
Gnomad	rs398123208
Varsome	rs398123208
LitVar	rs398123208
Map	rs398123208
PheGenI	rs398123208
Biobank	rs398123208
1000 genomes	rs398123208
hgdp	rs398123208
ensembl	rs398123208
geneview	rs398123208
scholar	rs398123208
google	rs398123208
pharmgkb	rs398123208
gwascentral	rs398123208
openSNP	rs398123208
23andMe	rs398123208
SNPshot	rs398123208
SNPdbe	rs398123208
MSV3d	rs398123208
GWAS Ctlg	rs398123208

Max Magnitude

0

ClinVar
Risk	rs398123208(A;A)
Alt	rs398123208(A;A)
Reference	Rs398123208(G;G)
Significance	Pathogenic
Disease	Fabry disease not provided
Variation	info
Gene	RPL36A-HNRNPH2 GLA
CLNDBN	Fabry disease not provided
Reversed	1
HGVS	NC_000023.10:g.100658926C>T
CLNSRC	HGMD
CLNACC	RCV000078273.4, RCV000157886.2,