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rs794728985

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728985(C;T)
Make rs794728985(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position219420591
GeneDES
is asnp
is mentioned by
dbSNPrs794728985
ebirs794728985
HLIrs794728985
Exacrs794728985
Varsomers794728985
Maprs794728985
PheGenIrs794728985
hapmaprs794728985
1000 genomesrs794728985
hgdprs794728985
ensemblrs794728985
gopubmedrs794728985
geneviewrs794728985
scholarrs794728985
googlers794728985
pharmgkbrs794728985
gwascentralrs794728985
openSNPrs794728985
23andMers794728985
23andMe allrs794728985
SNP Nexus

SNPshotrs794728985
SNPdbers794728985
MSV3drs794728985
GWAS Ctlgrs794728985
Max Magnitude0
ClinVar
Risk rs794728985(T;T)
Alt rs794728985(T;T)
Reference rs794728985(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene DES
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.220285313C>T
CLNSRC
CLNACC RCV000183349.2,