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rs797045586

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045586(A;A)
Make rs797045586(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position70972666
GeneFOXP1
is asnp
is mentioned by
dbSNPrs797045586
ebirs797045586
HLIrs797045586
Exacrs797045586
Varsomers797045586
Maprs797045586
PheGenIrs797045586
hapmaprs797045586
1000 genomesrs797045586
hgdprs797045586
ensemblrs797045586
gopubmedrs797045586
geneviewrs797045586
scholarrs797045586
googlers797045586
pharmgkbrs797045586
gwascentralrs797045586
openSNPrs797045586
23andMers797045586
23andMe allrs797045586
SNP Nexus

SNPshotrs797045586
SNPdbers797045586
MSV3drs797045586
GWAS Ctlgrs797045586
Max Magnitude0
ClinVar
Risk rs797045586(A;A)
Alt rs797045586(A;A)
Reference rs797045586(G;G)
Significance Probable-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.71021817C>T
CLNSRC
CLNACC RCV000194178.1,