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rs121434607

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121434607(C;C)
Make rs121434607(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154439027
GeneGDI1
is asnp
is mentioned by
dbSNPrs121434607
ebirs121434607
HLIrs121434607
Exacrs121434607
Varsomers121434607
Maprs121434607
PheGenIrs121434607
hapmaprs121434607
1000 genomesrs121434607
hgdprs121434607
ensemblrs121434607
gopubmedrs121434607
geneviewrs121434607
scholarrs121434607
googlers121434607
pharmgkbrs121434607
gwascentralrs121434607
openSNPrs121434607
23andMers121434607
23andMe allrs121434607
SNP Nexus

SNPshotrs121434607
SNPdbers121434607
MSV3drs121434607
GWAS Ctlgrs121434607
Max Magnitude0
OMIM300104
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434607(C;C)
Alt rs121434607(C;C)
Reference rs121434607(T;T)
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.153667373T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012392.16,