Have questions? Visit https://www.reddit.com/r/SNPedia

rs727504773

From SNPedia

Orientationminus
Geno Mag Summary
(CAGTTA;CAGTTA) 0 common in clinvar
Make rs727504773(CAGTTA;GGCAACTTT)
Make rs727504773(GGCAACTTT;GGCAACTTT)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position101398565
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs727504773
ebirs727504773
HLIrs727504773
Exacrs727504773
Varsomers727504773
Maprs727504773
PheGenIrs727504773
hapmaprs727504773
1000 genomesrs727504773
hgdprs727504773
ensemblrs727504773
gopubmedrs727504773
geneviewrs727504773
scholarrs727504773
googlers727504773
pharmgkbrs727504773
gwascentralrs727504773
openSNPrs727504773
23andMers727504773
23andMe allrs727504773
SNP Nexus

SNPshotrs727504773
SNPdbers727504773
MSV3drs727504773
GWAS Ctlgrs727504773
Max Magnitude0
ClinVar
Risk rs727504773(GGCAACTTT;GGCAACTTT)
Alt rs727504773(GGCAACTTT;GGCAACTTT)
Reference rs727504773(CAGTTA;CAGTTA)
Significance Probable-Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100653553_100653558delinsAAAGTTGCC
CLNSRC
CLNACC RCV000156088.1,