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rs794728984

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728984(A;A)
Make rs794728984(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position219420336
GeneDES
is asnp
is mentioned by
dbSNPrs794728984
ebirs794728984
HLIrs794728984
Exacrs794728984
Varsomers794728984
Maprs794728984
PheGenIrs794728984
hapmaprs794728984
1000 genomesrs794728984
hgdprs794728984
ensemblrs794728984
gopubmedrs794728984
geneviewrs794728984
scholarrs794728984
googlers794728984
pharmgkbrs794728984
gwascentralrs794728984
openSNPrs794728984
23andMers794728984
23andMe allrs794728984
SNP Nexus

SNPshotrs794728984
SNPdbers794728984
MSV3drs794728984
GWAS Ctlgrs794728984
Max Magnitude0
ClinVar
Risk rs794728984(A;A)
Alt rs794728984(A;A)
Reference rs794728984(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene DES
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.220285058T>A
CLNSRC
CLNACC RCV000183346.2,