Have questions? Visit https://www.reddit.com/r/SNPedia

rs786200976

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786200976(-;-)
Make rs786200976(-;A)
Make rs786200976(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position114631608
GeneFOXP2
is asnp
is mentioned by
dbSNPrs786200976
ebirs786200976
HLIrs786200976
Exacrs786200976
Varsomers786200976
Maprs786200976
PheGenIrs786200976
hapmaprs786200976
1000 genomesrs786200976
hgdprs786200976
ensemblrs786200976
gopubmedrs786200976
geneviewrs786200976
scholarrs786200976
googlers786200976
pharmgkbrs786200976
gwascentralrs786200976
openSNPrs786200976
23andMers786200976
23andMe allrs786200976
SNP Nexus

SNPshotrs786200976
SNPdbers786200976
MSV3drs786200976
GWAS Ctlgrs786200976
Max Magnitude0
ClinVar
Risk rs786200976(A;A)
Alt rs786200976(A;A)
Reference rs786200976(;)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXP2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.114271663dupA
CLNSRC
CLNACC RCV000153269.3,