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

rs387906483

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906483(G;G)
Make rs387906483(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101403809
GeneCACNA1I, GLA
is asnp
is mentioned by
dbSNPrs387906483
ebirs387906483
HLIrs387906483
Exacrs387906483
Varsomers387906483
Maprs387906483
PheGenIrs387906483
hapmaprs387906483
1000 genomesrs387906483
hgdprs387906483
ensemblrs387906483
gopubmedrs387906483
geneviewrs387906483
scholarrs387906483
googlers387906483
pharmgkbrs387906483
gwascentralrs387906483
openSNPrs387906483
23andMers387906483
23andMe allrs387906483
SNP Nexus

SNPshotrs387906483
SNPdbers387906483
MSV3drs387906483
GWAS Ctlgrs387906483
Max Magnitude0
ClinVar
Risk rs387906483(G;G)
Alt rs387906483(G;G)
Reference Rs387906483(T;T)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100658797A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011485.4,