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rs794727155

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727155(A;A)
Make rs794727155(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position70977859
GeneFOXP1
is asnp
is mentioned by
dbSNPrs794727155
ebirs794727155
HLIrs794727155
Exacrs794727155
Varsomers794727155
Maprs794727155
PheGenIrs794727155
hapmaprs794727155
1000 genomesrs794727155
hgdprs794727155
ensemblrs794727155
gopubmedrs794727155
geneviewrs794727155
scholarrs794727155
googlers794727155
pharmgkbrs794727155
gwascentralrs794727155
openSNPrs794727155
23andMers794727155
23andMe allrs794727155
SNP Nexus

SNPshotrs794727155
SNPdbers794727155
MSV3drs794727155
GWAS Ctlgrs794727155
Max Magnitude0
ClinVar
Risk rs794727155(A;A)
Alt rs794727155(A;A)
Reference rs794727155(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.71027010G>C; NC_000003.11:g.71027010G>T
CLNSRC
CLNACC RCV000207487.1, RCV000174956.1,