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rs1057517703

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517703(-;-)
Make rs1057517703(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position44290012
GeneAIRE
is asnp
is mentioned by
dbSNPrs1057517703
dbSNP (old)rs1057517703
ClinGenrs1057517703
ebirs1057517703
HLIrs1057517703
Exacrs1057517703
Gnomadrs1057517703
Varsomers1057517703
Maprs1057517703
PheGenIrs1057517703
Biobankrs1057517703
1000 genomesrs1057517703
hgdprs1057517703
ensemblrs1057517703
gopubmedrs1057517703
geneviewrs1057517703
scholarrs1057517703
googlers1057517703
pharmgkbrs1057517703
gwascentralrs1057517703
openSNPrs1057517703
23andMers1057517703
23andMe allrs1057517703
SNPshotrs1057517703
SNPdbers1057517703
MSV3drs1057517703
GWAS Ctlgrs1057517703
Max Magnitude0
ClinVar
Risk rs1057517703(-;-)
Alt rs1057517703(-;-)
Reference Rs1057517703(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene AIRE
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.45709895delC
CLNSRC
CLNACC RCV000414300.1,