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rs794728133

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728133(C;C)
Make rs794728133(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7585313
GeneDSP
is asnp
is mentioned by
dbSNPrs794728133
ebirs794728133
HLIrs794728133
Exacrs794728133
Varsomers794728133
Maprs794728133
PheGenIrs794728133
hapmaprs794728133
1000 genomesrs794728133
hgdprs794728133
ensemblrs794728133
gopubmedrs794728133
geneviewrs794728133
scholarrs794728133
googlers794728133
pharmgkbrs794728133
gwascentralrs794728133
openSNPrs794728133
23andMers794728133
23andMe allrs794728133
SNP Nexus

SNPshotrs794728133
SNPdbers794728133
MSV3drs794728133
GWAS Ctlgrs794728133
Max Magnitude0
ClinVar
Risk rs794728133(C;C)
Alt rs794728133(C;C)
Reference rs794728133(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7585546T>C
CLNSRC
CLNACC RCV000181348.1,