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rs587777380

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777380(G;G)
Make rs587777380(G;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position39830478
GeneDYRK1B, MIR6719
is asnp
is mentioned by
dbSNPrs587777380
ebirs587777380
HLIrs587777380
Exacrs587777380
Varsomers587777380
Maprs587777380
PheGenIrs587777380
hapmaprs587777380
1000 genomesrs587777380
hgdprs587777380
ensemblrs587777380
gopubmedrs587777380
geneviewrs587777380
scholarrs587777380
googlers587777380
pharmgkbrs587777380
gwascentralrs587777380
openSNPrs587777380
23andMers587777380
23andMe allrs587777380
SNP Nexus

SNPshotrs587777380
SNPdbers587777380
MSV3drs587777380
GWAS Ctlgrs587777380
Max Magnitude0
ClinVar
Risk rs587777380(G,T;G,T)
Alt rs587777380(G,T;G,T)
Reference rs587777380(A;A)
Significance Pathogenic
Disease Abdominal obesity-metabolic syndrome 3
Variation info
Gene MIR6719 DYRK1B
CLNDBN Abdominal obesity-metabolic syndrome 3
Reversed 1
HGVS NC_000019.9:g.40321118T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000119262.2,