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rs879253772

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs879253772(C;C)
Make rs879253772(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position114659617
GeneFOXP2
is asnp
is mentioned by
dbSNPrs879253772
ebirs879253772
HLIrs879253772
Exacrs879253772
Varsomers879253772
Maprs879253772
PheGenIrs879253772
hapmaprs879253772
1000 genomesrs879253772
hgdprs879253772
ensemblrs879253772
gopubmedrs879253772
geneviewrs879253772
scholarrs879253772
googlers879253772
pharmgkbrs879253772
gwascentralrs879253772
openSNPrs879253772
23andMers879253772
23andMe allrs879253772
SNP Nexus

SNPshotrs879253772
SNPdbers879253772
MSV3drs879253772
GWAS Ctlgrs879253772
Max Magnitude0
ClinVar
Risk rs879253772(C;C)
Alt rs879253772(C;C)
Reference rs879253772(T;T)
Significance Pathogenic
Disease Speech-language disorder 1
Variation info
Gene FOXP2
CLNDBN Speech-language disorder 1
Reversed 0
HGVS NC_000007.13:g.114299672T>C
CLNSRC
CLNACC RCV000234952.1,