Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs782377881

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs782377881(G;T)
Make rs782377881(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position49256801
GeneFOXP3
is asnp
is mentioned by
dbSNPrs782377881
dbSNP (old)rs782377881
ClinGenrs782377881
ebirs782377881
HLIrs782377881
Exacrs782377881
Gnomadrs782377881
Varsomers782377881
Maprs782377881
PheGenIrs782377881
Biobankrs782377881
1000 genomesrs782377881
hgdprs782377881
ensemblrs782377881
gopubmedrs782377881
geneviewrs782377881
scholarrs782377881
googlers782377881
pharmgkbrs782377881
gwascentralrs782377881
openSNPrs782377881
23andMers782377881
23andMe allrs782377881
SNPshotrs782377881
SNPdbers782377881
MSV3drs782377881
GWAS Ctlgrs782377881
Max Magnitude0
ClinVar
Risk rs782377881(A;A) rs782377881(T;T)
Alt rs782377881(A;A) rs782377881(T;T)
Reference Rs782377881(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXP3
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.49113258G>T
CLNSRC
CLNACC RCV000478450.1,