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rs1057524152

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524152(C;G)
Make rs1057524152(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position70976965
GeneFOXP1
is asnp
is mentioned by
dbSNPrs1057524152
dbSNP (classic)rs1057524152
ClinGenrs1057524152
ebirs1057524152
HLIrs1057524152
Exacrs1057524152
Gnomadrs1057524152
Varsomers1057524152
LitVarrs1057524152
Maprs1057524152
PheGenIrs1057524152
Biobankrs1057524152
1000 genomesrs1057524152
hgdprs1057524152
ensemblrs1057524152
geneviewrs1057524152
scholarrs1057524152
googlers1057524152
pharmgkbrs1057524152
gwascentralrs1057524152
openSNPrs1057524152
23andMers1057524152
23andMe allrs1057524152
SNPshotrs1057524152
SNPdbers1057524152
MSV3drs1057524152
GWAS Ctlgrs1057524152
Max Magnitude0
ClinVar
Risk rs1057524152(G;G)
Alt rs1057524152(G;G)
Reference Rs1057524152(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXP1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.71026116G>C
CLNSRC
CLNACC RCV000429800.1,