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rs201649896

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs201649896(A;T)
Make rs201649896(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position114426561
GeneFOXP2
is asnp
is mentioned by
dbSNPrs201649896
ebirs201649896
HLIrs201649896
Exacrs201649896
Varsomers201649896
Maprs201649896
PheGenIrs201649896
hapmaprs201649896
1000 genomesrs201649896
hgdprs201649896
ensemblrs201649896
gopubmedrs201649896
geneviewrs201649896
scholarrs201649896
googlers201649896
pharmgkbrs201649896
gwascentralrs201649896
openSNPrs201649896
23andMers201649896
23andMe allrs201649896
SNP Nexus

SNPshotrs201649896
SNPdbers201649896
MSV3drs201649896
GWAS Ctlgrs201649896
Max Magnitude0
ClinVar
Risk rs201649896(T;T)
Alt rs201649896(T;T)
Reference rs201649896(A;A)
Significance Pathogenic
Disease not provided Speech-language disorder 1
Variation info
Gene FOXP2
CLNDBN not provided Speech-language disorder 1
Reversed 0
HGVS NC_000007.13:g.114066616A>T
CLNSRC
CLNACC RCV000175859.1, RCV000234933.1,