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rs794728986

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728986(G;G)
Make rs794728986(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position219420642
GeneDES
is asnp
is mentioned by
dbSNPrs794728986
dbSNP (old)rs794728986
ClinGenrs794728986
ebirs794728986
HLIrs794728986
Exacrs794728986
Gnomadrs794728986
Varsomers794728986
Maprs794728986
PheGenIrs794728986
Biobankrs794728986
1000 genomesrs794728986
hgdprs794728986
ensemblrs794728986
gopubmedrs794728986
geneviewrs794728986
scholarrs794728986
googlers794728986
pharmgkbrs794728986
gwascentralrs794728986
openSNPrs794728986
23andMers794728986
23andMe allrs794728986
SNPshotrs794728986
SNPdbers794728986
MSV3drs794728986
GWAS Ctlgrs794728986
Max Magnitude0
ClinVar
Risk rs794728986(G;G)
Alt rs794728986(G;G)
Reference Rs794728986(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DES
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.220285364T>G
CLNSRC
CLNACC RCV000183350.1,