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rs869025202

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025202(A;G)
Make rs869025202(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position70977678
GeneFOXP1
is asnp
is mentioned by
dbSNPrs869025202
ebirs869025202
HLIrs869025202
Exacrs869025202
Varsomers869025202
Maprs869025202
PheGenIrs869025202
hapmaprs869025202
1000 genomesrs869025202
hgdprs869025202
ensemblrs869025202
gopubmedrs869025202
geneviewrs869025202
scholarrs869025202
googlers869025202
pharmgkbrs869025202
gwascentralrs869025202
openSNPrs869025202
23andMers869025202
23andMe allrs869025202
SNP Nexus

SNPshotrs869025202
SNPdbers869025202
MSV3drs869025202
GWAS Ctlgrs869025202
Max Magnitude0
ClinVar
Risk rs869025202(G;G)
Alt rs869025202(G;G)
Reference rs869025202(A;A)
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.71026829T>C
CLNSRC
CLNACC RCV000207489.1,