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rs111422676

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111422676(A;A)
Make rs111422676(A;G)
ReferenceGRCh38.p7 38.3/149
ChromosomeX
Position101398011
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs111422676
dbSNP (old)rs111422676
ClinGenrs111422676
ebirs111422676
HLIrs111422676
Exacrs111422676
Gnomadrs111422676
Varsomers111422676
Maprs111422676
PheGenIrs111422676
Biobankrs111422676
1000 genomesrs111422676
hgdprs111422676
ensemblrs111422676
gopubmedrs111422676
geneviewrs111422676
scholarrs111422676
googlers111422676
pharmgkbrs111422676
gwascentralrs111422676
openSNPrs111422676
23andMers111422676
23andMe allrs111422676
SNPshotrs111422676
SNPdbers111422676
MSV3drs111422676
GWAS Ctlgrs111422676
Max Magnitude0
ClinVar
Risk rs111422676(A;A)
Alt rs111422676(A;A)
Reference Rs111422676(G;G)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100652999C>T
CLNSRC
CLNACC RCV000398396.1,