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rs869025203

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025203(C;T)
Make rs869025203(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position70972667
GeneFOXP1
is asnp
is mentioned by
dbSNPrs869025203
ebirs869025203
HLIrs869025203
Exacrs869025203
Varsomers869025203
Maprs869025203
PheGenIrs869025203
hapmaprs869025203
1000 genomesrs869025203
hgdprs869025203
ensemblrs869025203
gopubmedrs869025203
geneviewrs869025203
scholarrs869025203
googlers869025203
pharmgkbrs869025203
gwascentralrs869025203
openSNPrs869025203
23andMers869025203
23andMe allrs869025203
SNP Nexus

SNPshotrs869025203
SNPdbers869025203
MSV3drs869025203
GWAS Ctlgrs869025203
Max Magnitude0
ClinVar
Risk rs869025203(T;T)
Alt rs869025203(T;T)
Reference rs869025203(C;C)
Significance Pathogenic
Disease Mental retardation with language impairment and with or without autistic features
Variation info
Gene FOXP1
CLNDBN Mental retardation with language impairment and with or without autistic features
Reversed 1
HGVS NC_000003.11:g.71021818G>A
CLNSRC
CLNACC RCV000207490.1,