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rs1064795069

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position49251734
GeneFOXP3
is asnp
is mentioned by
dbSNPrs1064795069
dbSNP (old)rs1064795069
ClinGenrs1064795069
ebirs1064795069
HLIrs1064795069
Exacrs1064795069
Gnomadrs1064795069
Varsomers1064795069
Maprs1064795069
PheGenIrs1064795069
Biobankrs1064795069
1000 genomesrs1064795069
hgdprs1064795069
ensemblrs1064795069
gopubmedrs1064795069
geneviewrs1064795069
scholarrs1064795069
googlers1064795069
pharmgkbrs1064795069
gwascentralrs1064795069
openSNPrs1064795069
23andMers1064795069
23andMe allrs1064795069
SNPshotrs1064795069
SNPdbers1064795069
MSV3drs1064795069
GWAS Ctlgrs1064795069
Max Magnitude0
ClinVar
Risk rs1064795069(T;T)
Alt rs1064795069(T;T)
Reference Rs1064795069(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXP3
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.49108195G>A
CLNSRC
CLNACC RCV000486769.1,