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rs797045019

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045019(C;T)
Make rs797045019(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position123668239
GeneTHOC2
is asnp
is mentioned by
dbSNPrs797045019
ebirs797045019
HLIrs797045019
Exacrs797045019
Varsomers797045019
Maprs797045019
PheGenIrs797045019
hapmaprs797045019
1000 genomesrs797045019
hgdprs797045019
ensemblrs797045019
gopubmedrs797045019
geneviewrs797045019
scholarrs797045019
googlers797045019
pharmgkbrs797045019
gwascentralrs797045019
openSNPrs797045019
23andMers797045019
23andMe allrs797045019
SNP Nexus

SNPshotrs797045019
SNPdbers797045019
MSV3drs797045019
GWAS Ctlgrs797045019
Max Magnitude0
ClinVar
Risk rs797045019(T;T)
Alt rs797045019(T;T)
Reference rs797045019(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene THOC2
CLNDBN Mental retardation, X-linked 12
Reversed 1
HGVS NC_000023.10:g.122802090G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000190531.2,