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rs1064793842

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;G) 3 speech and other processing issues possible
(G;G) 0 common in clinvar


Make rs1064793842(-;-)
Chromosome7
Position114662140
GeneFOXP2
is asnp
is mentioned by
dbSNPrs1064793842
dbSNP (old)rs1064793842
ClinGenrs1064793842
ebirs1064793842
HLIrs1064793842
Exacrs1064793842
Gnomadrs1064793842
Varsomers1064793842
LitVarrs1064793842
Maprs1064793842
PheGenIrs1064793842
Biobankrs1064793842
1000 genomesrs1064793842
hgdprs1064793842
ensemblrs1064793842
gopubmedrs1064793842
geneviewrs1064793842
scholarrs1064793842
googlers1064793842
pharmgkbrs1064793842
gwascentralrs1064793842
openSNPrs1064793842
23andMers1064793842
23andMe allrs1064793842
SNPshotrs1064793842
SNPdbers1064793842
MSV3drs1064793842
GWAS Ctlgrs1064793842
Max Magnitude3
ClinVar
Risk rs1064793842(-;-)
Alt rs1064793842(-;-)
Reference Rs1064793842(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXP2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.114302195delG
CLNSRC
CLNACC RCV000478073.1,