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rs797045021

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797045021(C;C)
Make rs797045021(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position123631770
GeneTHOC2
is asnp
is mentioned by
dbSNPrs797045021
ebirs797045021
HLIrs797045021
Exacrs797045021
Varsomers797045021
Maprs797045021
PheGenIrs797045021
hapmaprs797045021
1000 genomesrs797045021
hgdprs797045021
ensemblrs797045021
gopubmedrs797045021
geneviewrs797045021
scholarrs797045021
googlers797045021
pharmgkbrs797045021
gwascentralrs797045021
openSNPrs797045021
23andMers797045021
23andMe allrs797045021
SNP Nexus

SNPshotrs797045021
SNPdbers797045021
MSV3drs797045021
GWAS Ctlgrs797045021
Max Magnitude0
ClinVar
Risk rs797045021(C;C)
Alt rs797045021(C;C)
Reference rs797045021(T;T)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene THOC2
CLNDBN Mental retardation, X-linked 12
Reversed 1
HGVS NC_000023.10:g.122765621A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000190533.2,