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rs797044525

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044525(G;G)
Make rs797044525(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position37490244
GeneDYRK1A, LOC105372797
is asnp
is mentioned by
dbSNPrs797044525
ebirs797044525
HLIrs797044525
Exacrs797044525
Varsomers797044525
Maprs797044525
PheGenIrs797044525
hapmaprs797044525
1000 genomesrs797044525
hgdprs797044525
ensemblrs797044525
gopubmedrs797044525
geneviewrs797044525
scholarrs797044525
googlers797044525
pharmgkbrs797044525
gwascentralrs797044525
openSNPrs797044525
23andMers797044525
23andMe allrs797044525
SNP Nexus

SNPshotrs797044525
SNPdbers797044525
MSV3drs797044525
GWAS Ctlgrs797044525
Max Magnitude0
ClinVar
Risk rs797044525(G;G)
Alt rs797044525(G;G)
Reference rs797044525(T;T)
Significance Probable-Pathogenic
Disease Mental retardation
Variation info
Gene DYRK1A
CLNDBN Mental retardation, autosomal dominant 7
Reversed 0
HGVS NC_000021.8:g.38862546T>G
CLNSRC UCLA
CLNACC RCV000190484.1,