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rs879253770

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs879253770(-;-)
Make rs879253770(-;ACAACAGCAGCA)
Make rs879253770(ACAACAGCAGCA;ACAACAGCAGCA)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position114629914
GeneFOXP2
is asnp
is mentioned by
dbSNPrs879253770
ebirs879253770
HLIrs879253770
Exacrs879253770
Varsomers879253770
Maprs879253770
PheGenIrs879253770
hapmaprs879253770
1000 genomesrs879253770
hgdprs879253770
ensemblrs879253770
gopubmedrs879253770
geneviewrs879253770
scholarrs879253770
googlers879253770
pharmgkbrs879253770
gwascentralrs879253770
openSNPrs879253770
23andMers879253770
23andMe allrs879253770
SNP Nexus

SNPshotrs879253770
SNPdbers879253770
MSV3drs879253770
GWAS Ctlgrs879253770
Max Magnitude0
ClinVar
Risk rs879253770(CAGCAGCAACAA;CAGCAGCAACAA)
Alt rs879253770(CAGCAGCAACAA;CAGCAGCAACAA)
Reference rs879253770(;)
Significance Pathogenic
Disease Speech-language disorder 1
Variation info
Gene FOXP2
CLNDBN Speech-language disorder 1
Reversed 0
HGVS NC_000007.13:g.114269958_114269969dupACAACAGCAGCA
CLNSRC
CLNACC RCV000234942.1,