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rs797045018

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797045018(C;C)
Make rs797045018(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position123665715
GeneTHOC2
is asnp
is mentioned by
dbSNPrs797045018
ebirs797045018
HLIrs797045018
Exacrs797045018
Varsomers797045018
Maprs797045018
PheGenIrs797045018
hapmaprs797045018
1000 genomesrs797045018
hgdprs797045018
ensemblrs797045018
gopubmedrs797045018
geneviewrs797045018
scholarrs797045018
googlers797045018
pharmgkbrs797045018
gwascentralrs797045018
openSNPrs797045018
23andMers797045018
23andMe allrs797045018
SNP Nexus

SNPshotrs797045018
SNPdbers797045018
MSV3drs797045018
GWAS Ctlgrs797045018
Max Magnitude0
ClinVar
Risk rs797045018(C;C)
Alt rs797045018(C;C)
Reference rs797045018(T;T)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene THOC2
CLNDBN Mental retardation, X-linked 12
Reversed 1
HGVS NC_000023.10:g.122799566A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000190530.2,