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rs797044652

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044652(-;C)
Make rs797044652(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position70977935
GeneFOXP1
is asnp
is mentioned by
dbSNPrs797044652
ClinGenrs797044652
ebirs797044652
HLIrs797044652
Exacrs797044652
Varsomers797044652
Maprs797044652
PheGenIrs797044652
hapmaprs797044652
1000 genomesrs797044652
hgdprs797044652
ensemblrs797044652
gopubmedrs797044652
geneviewrs797044652
scholarrs797044652
googlers797044652
pharmgkbrs797044652
gwascentralrs797044652
openSNPrs797044652
23andMers797044652
23andMe allrs797044652
SNP Nexus

SNPshotrs797044652
SNPdbers797044652
MSV3drs797044652
GWAS Ctlgrs797044652
Max Magnitude0
ClinVar
Risk rs797044652(C;C)
Alt rs797044652(C;C)
Reference Rs797044652(-;-)
Significance Pathogenic
Disease Mental retardation with language impairment and with or without autistic features not provided
Variation info
Gene FOXP1
CLNDBN Mental retardation with language impairment and with or without autistic features not provided
Reversed 1
HGVS NC_000003.11:g.71027087dupG
CLNSRC
CLNACC RCV000174957.1, RCV000352326.1,