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rs398122917

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122917(C;G)
Make rs398122917(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position155280059
GeneCLIC2
is asnp
is mentioned by
dbSNPrs398122917
ebirs398122917
HLIrs398122917
Exacrs398122917
Varsomers398122917
Maprs398122917
PheGenIrs398122917
hapmaprs398122917
1000 genomesrs398122917
hgdprs398122917
ensemblrs398122917
gopubmedrs398122917
geneviewrs398122917
scholarrs398122917
googlers398122917
pharmgkbrs398122917
gwascentralrs398122917
openSNPrs398122917
23andMers398122917
23andMe allrs398122917
SNP Nexus

SNPshotrs398122917
SNPdbers398122917
MSV3drs398122917
GWAS Ctlgrs398122917
Max Magnitude0
ClinVar
Risk rs398122917(G;G)
Alt rs398122917(G;G)
Reference rs398122917(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene CLIC2
CLNDBN Mental retardation, X-linked, syndromic 32
Reversed 1
HGVS NC_000023.10:g.154509348G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000033043.15,