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rs766476648

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs766476648(A;C)
Make rs766476648(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position114663469
GeneFOXP2
is asnp
is mentioned by
dbSNPrs766476648
ebirs766476648
HLIrs766476648
Exacrs766476648
Varsomers766476648
Maprs766476648
PheGenIrs766476648
hapmaprs766476648
1000 genomesrs766476648
hgdprs766476648
ensemblrs766476648
gopubmedrs766476648
geneviewrs766476648
scholarrs766476648
googlers766476648
pharmgkbrs766476648
gwascentralrs766476648
openSNPrs766476648
23andMers766476648
23andMe allrs766476648
SNP Nexus

SNPshotrs766476648
SNPdbers766476648
MSV3drs766476648
GWAS Ctlgrs766476648
Max Magnitude0
ClinVar
Risk rs766476648(C;C)
Alt rs766476648(C;C)
Reference rs766476648(A;A)
Significance Pathogenic
Disease Speech-language disorder 1
Variation info
Gene FOXP2
CLNDBN Speech-language disorder 1
Reversed 0
HGVS NC_000007.13:g.114303524A>C
CLNSRC
CLNACC RCV000234955.1,