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rs780441716

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs780441716(C;T)
Make rs780441716(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position37490201
GeneDYRK1A, LOC105372797
is asnp
is mentioned by
dbSNPrs780441716
dbSNP (classic)rs780441716
ClinGenrs780441716
ebirs780441716
HLIrs780441716
Exacrs780441716
Gnomadrs780441716
Varsomers780441716
LitVarrs780441716
Maprs780441716
PheGenIrs780441716
Biobankrs780441716
1000 genomesrs780441716
hgdprs780441716
ensemblrs780441716
geneviewrs780441716
scholarrs780441716
googlers780441716
pharmgkbrs780441716
gwascentralrs780441716
openSNPrs780441716
23andMers780441716
SNPshotrs780441716
SNPdbers780441716
MSV3drs780441716
GWAS Ctlgrs780441716
Max Magnitude0
ClinVar
Risk rs780441716(T;T)
Alt rs780441716(T;T)
Reference Rs780441716(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DYRK1A
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.38862503C>T
CLNSRC
CLNACC RCV000481862.1,