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rs150634562

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150634562(A;A)
Make rs150634562(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome21
Position44291116
GeneAIRE
is asnp
is mentioned by
dbSNPrs150634562
dbSNP (old)rs150634562
ClinGenrs150634562
ebirs150634562
HLIrs150634562
Exacrs150634562
Gnomadrs150634562
Varsomers150634562
LitVarrs150634562
Maprs150634562
PheGenIrs150634562
Biobankrs150634562
1000 genomesrs150634562
hgdprs150634562
ensemblrs150634562
gopubmedrs150634562
geneviewrs150634562
scholarrs150634562
googlers150634562
pharmgkbrs150634562
gwascentralrs150634562
openSNPrs150634562
23andMers150634562
23andMe allrs150634562
SNPshotrs150634562
SNPdbers150634562
MSV3drs150634562
GWAS Ctlgrs150634562
Max Magnitude0
ClinVar
Risk rs150634562(A;A)
Alt rs150634562(A;A)
Reference Rs150634562(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AIRE
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.45710999G>A
CLNSRC
CLNACC RCV000254752.2,