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rs794728119

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728119(C;T)
Make rs794728119(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7580151
GeneDSP
is asnp
is mentioned by
dbSNPrs794728119
ebirs794728119
HLIrs794728119
Exacrs794728119
Varsomers794728119
Maprs794728119
PheGenIrs794728119
hapmaprs794728119
1000 genomesrs794728119
hgdprs794728119
ensemblrs794728119
gopubmedrs794728119
geneviewrs794728119
scholarrs794728119
googlers794728119
pharmgkbrs794728119
gwascentralrs794728119
openSNPrs794728119
23andMers794728119
23andMe allrs794728119
SNP Nexus

SNPshotrs794728119
SNPdbers794728119
MSV3drs794728119
GWAS Ctlgrs794728119
Max Magnitude0
ClinVar
Risk rs794728119(T;T)
Alt rs794728119(T;T)
Reference rs794728119(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7580384C>T
CLNSRC
CLNACC RCV000181309.1,