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rs1057517736

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517736(C;T)
Make rs1057517736(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position49253161
GeneFOXP3
is asnp
is mentioned by
dbSNPrs1057517736
dbSNP (old)rs1057517736
ClinGenrs1057517736
ebirs1057517736
HLIrs1057517736
Exacrs1057517736
Gnomadrs1057517736
Varsomers1057517736
Maprs1057517736
PheGenIrs1057517736
Biobankrs1057517736
1000 genomesrs1057517736
hgdprs1057517736
ensemblrs1057517736
gopubmedrs1057517736
geneviewrs1057517736
scholarrs1057517736
googlers1057517736
pharmgkbrs1057517736
gwascentralrs1057517736
openSNPrs1057517736
23andMers1057517736
23andMe allrs1057517736
SNPshotrs1057517736
SNPdbers1057517736
MSV3drs1057517736
GWAS Ctlgrs1057517736
Max Magnitude0
ClinVar
Risk rs1057517736(T;T)
Alt rs1057517736(T;T)
Reference Rs1057517736(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXP3
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.49109622G>A
CLNSRC
CLNACC RCV000413665.1,