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rs794728113

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728113(G;T)
Make rs794728113(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7569279
GeneDSP
is asnp
is mentioned by
dbSNPrs794728113
ebirs794728113
HLIrs794728113
Exacrs794728113
Varsomers794728113
Maprs794728113
PheGenIrs794728113
hapmaprs794728113
1000 genomesrs794728113
hgdprs794728113
ensemblrs794728113
gopubmedrs794728113
geneviewrs794728113
scholarrs794728113
googlers794728113
pharmgkbrs794728113
gwascentralrs794728113
openSNPrs794728113
23andMers794728113
23andMe allrs794728113
SNP Nexus

SNPshotrs794728113
SNPdbers794728113
MSV3drs794728113
GWAS Ctlgrs794728113
Max Magnitude0
ClinVar
Risk rs794728113(T;T)
Alt rs794728113(T;T)
Reference rs794728113(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7569512G>T
CLNSRC
CLNACC RCV000181291.1,