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rs794728994

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728994(G;G)
Make rs794728994(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position219418826
GeneDES
is asnp
is mentioned by
dbSNPrs794728994
ebirs794728994
HLIrs794728994
Exacrs794728994
Varsomers794728994
Maprs794728994
PheGenIrs794728994
hapmaprs794728994
1000 genomesrs794728994
hgdprs794728994
ensemblrs794728994
gopubmedrs794728994
geneviewrs794728994
scholarrs794728994
googlers794728994
pharmgkbrs794728994
gwascentralrs794728994
openSNPrs794728994
23andMers794728994
23andMe allrs794728994
SNP Nexus

SNPshotrs794728994
SNPdbers794728994
MSV3drs794728994
GWAS Ctlgrs794728994
Max Magnitude0
ClinVar
Risk rs794728994(G;G)
Alt rs794728994(G;G)
Reference rs794728994(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DES
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.220283548T>G
CLNSRC
CLNACC RCV000183370.1,