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rs869312708

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312708(C;T)
Make rs869312708(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position37506191
GeneDYRK1A
is asnp
is mentioned by
dbSNPrs869312708
ebirs869312708
HLIrs869312708
Exacrs869312708
Varsomers869312708
Maprs869312708
PheGenIrs869312708
hapmaprs869312708
1000 genomesrs869312708
hgdprs869312708
ensemblrs869312708
gopubmedrs869312708
geneviewrs869312708
scholarrs869312708
googlers869312708
pharmgkbrs869312708
gwascentralrs869312708
openSNPrs869312708
23andMers869312708
23andMe allrs869312708
SNP Nexus

SNPshotrs869312708
SNPdbers869312708
MSV3drs869312708
GWAS Ctlgrs869312708
Max Magnitude0
ClinVar
Risk rs869312708(T;T)
Alt rs869312708(T;T)
Reference rs869312708(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene DYRK1A
CLNDBN Mental retardation, autosomal dominant 7
Reversed 0
HGVS NC_000021.8:g.38878494C>T
CLNSRC
CLNACC RCV000209829.1,