Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728988

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728988(C;C)
Make rs794728988(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position219421521
GeneDES
is asnp
is mentioned by
dbSNPrs794728988
ebirs794728988
HLIrs794728988
Exacrs794728988
Varsomers794728988
Maprs794728988
PheGenIrs794728988
hapmaprs794728988
1000 genomesrs794728988
hgdprs794728988
ensemblrs794728988
gopubmedrs794728988
geneviewrs794728988
scholarrs794728988
googlers794728988
pharmgkbrs794728988
gwascentralrs794728988
openSNPrs794728988
23andMers794728988
23andMe allrs794728988
SNP Nexus

SNPshotrs794728988
SNPdbers794728988
MSV3drs794728988
GWAS Ctlgrs794728988
Max Magnitude0
ClinVar
Risk rs794728988(C;C)
Alt rs794728988(C;C)
Reference rs794728988(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DES
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.220286243T>C
CLNSRC
CLNACC RCV000183355.2,