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rs794728993

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728993(C;T)
Make rs794728993(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position219418775
GeneDES
is asnp
is mentioned by
dbSNPrs794728993
ebirs794728993
HLIrs794728993
Exacrs794728993
Varsomers794728993
Maprs794728993
PheGenIrs794728993
hapmaprs794728993
1000 genomesrs794728993
hgdprs794728993
ensemblrs794728993
gopubmedrs794728993
geneviewrs794728993
scholarrs794728993
googlers794728993
pharmgkbrs794728993
gwascentralrs794728993
openSNPrs794728993
23andMers794728993
23andMe allrs794728993
SNP Nexus

SNPshotrs794728993
SNPdbers794728993
MSV3drs794728993
GWAS Ctlgrs794728993
Max Magnitude0
ClinVar
Risk rs794728993(T;T)
Alt rs794728993(T;T)
Reference rs794728993(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DES
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.220283497C>T
CLNSRC
CLNACC RCV000183369.1,