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rs869312678

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs869312678(-;-)
Make rs869312678(-;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position42209920
GeneTCF20
is asnp
is mentioned by
dbSNPrs869312678
ebirs869312678
HLIrs869312678
Exacrs869312678
Varsomers869312678
Maprs869312678
PheGenIrs869312678
hapmaprs869312678
1000 genomesrs869312678
hgdprs869312678
ensemblrs869312678
gopubmedrs869312678
geneviewrs869312678
scholarrs869312678
googlers869312678
pharmgkbrs869312678
gwascentralrs869312678
openSNPrs869312678
23andMers869312678
23andMe allrs869312678
SNP Nexus

SNPshotrs869312678
SNPdbers869312678
MSV3drs869312678
GWAS Ctlgrs869312678
Max Magnitude0
ClinVar
Risk rs869312678(;)
Alt rs869312678(;)
Reference rs869312678(TG;TG)
Significance Pathogenic
Disease Autistic behavior Delayed speech and language development Intellectual disability (moderate)
Variation info
Gene TCF20
CLNDBN Autistic behavior Delayed speech and language development Intellectual disability (moderate)
Reversed 1
HGVS NC_000022.10:g.42605926_42605927delCA
CLNSRC
CLNACC RCV000209874.3,