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rs1064793130

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Chromosome3
Position70977935
GeneFOXP1
is asnp
is mentioned by
dbSNPrs1064793130
dbSNP (old)rs1064793130
ClinGenrs1064793130
ebirs1064793130
HLIrs1064793130
Exacrs1064793130
Gnomadrs1064793130
Varsomers1064793130
LitVarrs1064793130
Maprs1064793130
PheGenIrs1064793130
Biobankrs1064793130
1000 genomesrs1064793130
hgdprs1064793130
ensemblrs1064793130
gopubmedrs1064793130
geneviewrs1064793130
scholarrs1064793130
googlers1064793130
pharmgkbrs1064793130
gwascentralrs1064793130
openSNPrs1064793130
23andMers1064793130
23andMe allrs1064793130
SNPshotrs1064793130
SNPdbers1064793130
MSV3drs1064793130
GWAS Ctlgrs1064793130
Max Magnitude0
ClinVar
Risk rs1064793130(-;-)
Alt rs1064793130(-;-)
Reference Rs1064793130(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXP1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.71027086_71027087delAG
CLNSRC
CLNACC RCV000484956.1,