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

rs1057518281

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518281(A;G)
Make rs1057518281(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position49251702
GeneFOXP3
is asnp
is mentioned by
dbSNPrs1057518281
dbSNP (old)rs1057518281
ClinGenrs1057518281
ebirs1057518281
HLIrs1057518281
Exacrs1057518281
Gnomadrs1057518281
Varsomers1057518281
LitVarrs1057518281
Maprs1057518281
PheGenIrs1057518281
Biobankrs1057518281
1000 genomesrs1057518281
hgdprs1057518281
ensemblrs1057518281
gopubmedrs1057518281
geneviewrs1057518281
scholarrs1057518281
googlers1057518281
pharmgkbrs1057518281
gwascentralrs1057518281
openSNPrs1057518281
23andMers1057518281
23andMe allrs1057518281
SNPshotrs1057518281
SNPdbers1057518281
MSV3drs1057518281
GWAS Ctlgrs1057518281
Max Magnitude0
ClinVar
Risk rs1057518281(G;G)
Alt rs1057518281(G;G)
Reference Rs1057518281(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXP3
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.49108163T>C
CLNSRC
CLNACC RCV000414229.1,