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rs1057517878

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517878(C;C)
Make rs1057517878(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position44286032
GeneAIRE
is asnp
is mentioned by
dbSNPrs1057517878
dbSNP (old)rs1057517878
ClinGenrs1057517878
ebirs1057517878
HLIrs1057517878
Exacrs1057517878
Gnomadrs1057517878
Varsomers1057517878
Maprs1057517878
PheGenIrs1057517878
Biobankrs1057517878
1000 genomesrs1057517878
hgdprs1057517878
ensemblrs1057517878
gopubmedrs1057517878
geneviewrs1057517878
scholarrs1057517878
googlers1057517878
pharmgkbrs1057517878
gwascentralrs1057517878
openSNPrs1057517878
23andMers1057517878
23andMe allrs1057517878
SNPshotrs1057517878
SNPdbers1057517878
MSV3drs1057517878
GWAS Ctlgrs1057517878
Max Magnitude0
ClinVar
Risk rs1057517878(C;C)
Alt rs1057517878(C;C)
Reference Rs1057517878(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AIRE
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.45705915G>C
CLNSRC
CLNACC RCV000414619.1,