rs398123198

Orientation

minus

Stabilized

minus

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

Make rs398123198(-;-)

Make rs398123198(-;TC)

Reference

GRCh38 38.1/141

Chromosome

X

Position

101398065

Gene	GLA, RPL36A-HNRNPH2

is a	snp
is	mentioned by
dbSNP	rs398123198
dbSNP (classic)	rs398123198
ClinGen	rs398123198
ebi	rs398123198
HLI	rs398123198
Exac	rs398123198
Gnomad	rs398123198
Varsome	rs398123198
LitVar	rs398123198
Map	rs398123198
PheGenI	rs398123198
Biobank	rs398123198
1000 genomes	rs398123198
hgdp	rs398123198
ensembl	rs398123198
geneview	rs398123198
scholar	rs398123198
google	rs398123198
pharmgkb	rs398123198
gwascentral	rs398123198
openSNP	rs398123198
23andMe	rs398123198
SNPshot	rs398123198
SNPdbe	rs398123198
MSV3d	rs398123198
GWAS Ctlg	rs398123198

Max Magnitude

0

ClinVar
Risk	rs398123198(-;-)
Alt	rs398123198(-;-)
Reference	Rs398123198(TC;TC)
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.100653053_100653054delGA
CLNSRC	HGMD
CLNACC	RCV000078263.7, RCV000236755.1,