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rs1064796914

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Chromosome3
Position70977910
GeneFOXP1
is asnp
is mentioned by
dbSNPrs1064796914
dbSNP (old)rs1064796914
ClinGenrs1064796914
ebirs1064796914
HLIrs1064796914
Exacrs1064796914
Gnomadrs1064796914
Varsomers1064796914
Maprs1064796914
PheGenIrs1064796914
Biobankrs1064796914
1000 genomesrs1064796914
hgdprs1064796914
ensemblrs1064796914
gopubmedrs1064796914
geneviewrs1064796914
scholarrs1064796914
googlers1064796914
pharmgkbrs1064796914
gwascentralrs1064796914
openSNPrs1064796914
23andMers1064796914
23andMe allrs1064796914
SNPshotrs1064796914
SNPdbers1064796914
MSV3drs1064796914
GWAS Ctlgrs1064796914
Max Magnitude0
ClinVar
Risk rs1064796914(-;-)
Alt rs1064796914(-;-)
Reference Rs1064796914(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXP1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.71027061_71027062delAG
CLNSRC
CLNACC RCV000480148.1,