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rs376106351

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs376106351(C;T)
Make rs376106351(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position37506205
GeneDYRK1A
is asnp
is mentioned by
dbSNPrs376106351
dbSNP (classic)rs376106351
ClinGenrs376106351
ebirs376106351
HLIrs376106351
Exacrs376106351
Gnomadrs376106351
Varsomers376106351
LitVarrs376106351
Maprs376106351
PheGenIrs376106351
Biobankrs376106351
1000 genomesrs376106351
hgdprs376106351
ensemblrs376106351
geneviewrs376106351
scholarrs376106351
googlers376106351
pharmgkbrs376106351
gwascentralrs376106351
openSNPrs376106351
23andMers376106351
SNPshotrs376106351
SNPdbers376106351
MSV3drs376106351
GWAS Ctlgrs376106351
Max Magnitude0
ClinVar
Risk rs376106351(A;A) rs376106351(T;T)
Alt rs376106351(A;A) rs376106351(T;T)
Reference Rs376106351(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYRK1A
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.38878508C>A
CLNSRC
CLNACC RCV000481279.1,