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

rs1057524732

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524732(C;T)
Make rs1057524732(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position71047032
GeneFOXP1
is asnp
is mentioned by
dbSNPrs1057524732
dbSNP (old)rs1057524732
ClinGenrs1057524732
ebirs1057524732
HLIrs1057524732
Exacrs1057524732
Gnomadrs1057524732
Varsomers1057524732
Maprs1057524732
PheGenIrs1057524732
Biobankrs1057524732
1000 genomesrs1057524732
hgdprs1057524732
ensemblrs1057524732
gopubmedrs1057524732
geneviewrs1057524732
scholarrs1057524732
googlers1057524732
pharmgkbrs1057524732
gwascentralrs1057524732
openSNPrs1057524732
23andMers1057524732
23andMe allrs1057524732
SNPshotrs1057524732
SNPdbers1057524732
MSV3drs1057524732
GWAS Ctlgrs1057524732
Max Magnitude0
ClinVar
Risk rs1057524732(T;T)
Alt rs1057524732(T;T)
Reference Rs1057524732(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXP1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.71096183G>A
CLNSRC
CLNACC RCV000429050.1,