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rs1039571136

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1039571136(C;T)
Make rs1039571136(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position37490442
GeneDYRK1A, LOC105372797
is asnp
is mentioned by
dbSNPrs1039571136
dbSNP (old)rs1039571136
ClinGenrs1039571136
ebirs1039571136
HLIrs1039571136
Exacrs1039571136
Gnomadrs1039571136
Varsomers1039571136
Maprs1039571136
PheGenIrs1039571136
Biobankrs1039571136
1000 genomesrs1039571136
hgdprs1039571136
ensemblrs1039571136
gopubmedrs1039571136
geneviewrs1039571136
scholarrs1039571136
googlers1039571136
pharmgkbrs1039571136
gwascentralrs1039571136
openSNPrs1039571136
23andMers1039571136
23andMe allrs1039571136
SNPshotrs1039571136
SNPdbers1039571136
MSV3drs1039571136
GWAS Ctlgrs1039571136
Max Magnitude0
ClinVar
Risk rs1039571136(A;A)
Alt rs1039571136(A;A)
Reference Rs1039571136(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYRK1A
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.38862744C>T
CLNSRC
CLNACC RCV000438308.1,