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rs794728995

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728995(A;G)
Make rs794728995(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position219425698
GeneDES
is asnp
is mentioned by
dbSNPrs794728995
ebirs794728995
HLIrs794728995
Exacrs794728995
Varsomers794728995
Maprs794728995
PheGenIrs794728995
hapmaprs794728995
1000 genomesrs794728995
hgdprs794728995
ensemblrs794728995
gopubmedrs794728995
geneviewrs794728995
scholarrs794728995
googlers794728995
pharmgkbrs794728995
gwascentralrs794728995
openSNPrs794728995
23andMers794728995
23andMe allrs794728995
SNP Nexus

SNPshotrs794728995
SNPdbers794728995
MSV3drs794728995
GWAS Ctlgrs794728995
Max Magnitude0
ClinVar
Risk rs794728995(G;G)
Alt rs794728995(G;G)
Reference rs794728995(A;A)
Significance Pathogenic
Disease not specified
Variation info
Gene DES LOC101928568
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.220290420A>G
CLNSRC
CLNACC RCV000183376.2,