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

rs879253771

From SNPedia

Orientationplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs879253771(-;-)
Make rs879253771(-;CA)
Make rs879253771(CA;CA)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position114652276
GeneFOXP2, MIR3666
is asnp
is mentioned by
dbSNPrs879253771
ebirs879253771
HLIrs879253771
Exacrs879253771
Varsomers879253771
Maprs879253771
PheGenIrs879253771
hapmaprs879253771
1000 genomesrs879253771
hgdprs879253771
ensemblrs879253771
gopubmedrs879253771
geneviewrs879253771
scholarrs879253771
googlers879253771
pharmgkbrs879253771
gwascentralrs879253771
openSNPrs879253771
23andMers879253771
23andMe allrs879253771
SNP Nexus

SNPshotrs879253771
SNPdbers879253771
MSV3drs879253771
GWAS Ctlgrs879253771
Max Magnitude0
ClinVar
Risk rs879253771(;)
Alt rs879253771(;)
Reference rs879253771(AC;AC)
Significance Pathogenic
Disease Speech-language disorder 1
Variation info
Gene FOXP2 MIR3666
CLNDBN Speech-language disorder 1
Reversed 0
HGVS NC_000007.13:g.114292331_114292332delCA
CLNSRC
CLNACC RCV000234941.1,