Have questions? Visit https://www.reddit.com/r/SNPedia

rs797045584

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045584(C;T)
Make rs797045584(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position70976964
GeneFOXP1
is asnp
is mentioned by
dbSNPrs797045584
ebirs797045584
HLIrs797045584
Exacrs797045584
Varsomers797045584
Maprs797045584
PheGenIrs797045584
hapmaprs797045584
1000 genomesrs797045584
hgdprs797045584
ensemblrs797045584
gopubmedrs797045584
geneviewrs797045584
scholarrs797045584
googlers797045584
pharmgkbrs797045584
gwascentralrs797045584
openSNPrs797045584
23andMers797045584
23andMe allrs797045584
SNP Nexus

SNPshotrs797045584
SNPdbers797045584
MSV3drs797045584
GWAS Ctlgrs797045584
Max Magnitude0
ClinVar
Risk rs797045584(T;T)
Alt rs797045584(T;T)
Reference rs797045584(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.71026115G>A
CLNSRC
CLNACC RCV000195136.1,