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rs121434608

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434608(C;T)
Make rs121434608(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154438819
GeneGDI1
is asnp
is mentioned by
dbSNPrs121434608
ebirs121434608
HLIrs121434608
Exacrs121434608
Varsomers121434608
Maprs121434608
PheGenIrs121434608
hapmaprs121434608
1000 genomesrs121434608
hgdprs121434608
ensemblrs121434608
gopubmedrs121434608
geneviewrs121434608
scholarrs121434608
googlers121434608
pharmgkbrs121434608
gwascentralrs121434608
openSNPrs121434608
23andMers121434608
23andMe allrs121434608
SNP Nexus

SNPshotrs121434608
SNPdbers121434608
MSV3drs121434608
GWAS Ctlgrs121434608
Max Magnitude0
OMIM300104
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121434608(T;T)
Alt rs121434608(T;T)
Reference rs121434608(C;C)
Significance Pathogenic
Disease X-Linked Mental Retardation 41
Variation info
Gene GDI1
CLNDBN X-Linked Mental Retardation 41
Reversed 0
HGVS NC_000023.10:g.153667165C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012393.14,