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rs782511378

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs782511378(A;A)
Make rs782511378(A;G)
ReferenceGRCh38.p7 38.3/149
ChromosomeX
Position49257483
GeneFOXP3
is asnp
is mentioned by
dbSNPrs782511378
dbSNP (classic)rs782511378
ClinGenrs782511378
ebirs782511378
HLIrs782511378
Exacrs782511378
Gnomadrs782511378
Varsomers782511378
LitVarrs782511378
Maprs782511378
PheGenIrs782511378
Biobankrs782511378
1000 genomesrs782511378
hgdprs782511378
ensemblrs782511378
geneviewrs782511378
scholarrs782511378
googlers782511378
pharmgkbrs782511378
gwascentralrs782511378
openSNPrs782511378
23andMers782511378
SNPshotrs782511378
SNPdbers782511378
MSV3drs782511378
GWAS Ctlgrs782511378
Max Magnitude0
ClinVar
Risk rs782511378(A;A)
Alt rs782511378(A;A)
Reference Rs782511378(G;G)
Significance Probable-Pathogenic
Disease Diabetes mellitus type 1
Variation info
Gene FOXP3
CLNDBN Diabetes mellitus type 1
Reversed 0
HGVS NC_000023.10:g.49113940G>A
CLNSRC
CLNACC RCV000258798.1,