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

rs17137124

From SNPedia

Orientationplus
Stabilizedplus
Make rs17137124(C;C)
Make rs17137124(C;T)
Make rs17137124(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position114570759
GeneFOXP2
is asnp
is mentioned by
dbSNPrs17137124
ebirs17137124
HLIrs17137124
Exacrs17137124
Varsomers17137124
Maprs17137124
PheGenIrs17137124
hapmaprs17137124
1000 genomesrs17137124
hgdprs17137124
ensemblrs17137124
gopubmedrs17137124
geneviewrs17137124
scholarrs17137124
googlers17137124
pharmgkbrs17137124
gwascentralrs17137124
openSNPrs17137124
23andMers17137124
23andMe allrs17137124
SNP Nexus

SNPshotrs17137124
SNPdbers17137124
MSV3drs17137124
GWAS Ctlgrs17137124
GMAF0.4692
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 15877281OA-icon.png] variations in rs17137124 and rs10227893 may impair speech


[PMID 22129783] FOXP2, APOE, and PRNP: New Modulators in Primary Progressive Aphasia


[PMID 19997522OA-icon.png] Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment.


[PMID 20649982OA-icon.png] FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.


[PMID 20858950] The speech and language FOXP2 gene modulates the phenotype of frontotemporal lobar degeneration.


[PMID 20923434] Association between FOXP2 gene and speech sound disorder in Chinese population.