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rs794728157

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794728157(-;-)
Make rs794728157(-;TT)
Make rs794728157(TT;TT)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7578528
GeneDSP
is asnp
is mentioned by
dbSNPrs794728157
ebirs794728157
HLIrs794728157
Exacrs794728157
Varsomers794728157
Maprs794728157
PheGenIrs794728157
hapmaprs794728157
1000 genomesrs794728157
hgdprs794728157
ensemblrs794728157
gopubmedrs794728157
geneviewrs794728157
scholarrs794728157
googlers794728157
pharmgkbrs794728157
gwascentralrs794728157
openSNPrs794728157
23andMers794728157
23andMe allrs794728157
SNP Nexus

SNPshotrs794728157
SNPdbers794728157
MSV3drs794728157
GWAS Ctlgrs794728157
Max Magnitude0
ClinVar
Risk rs794728157(TT;TT)
Alt rs794728157(TT;TT)
Reference rs794728157(;)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7578760_7578761dupTT
CLNSRC
CLNACC RCV000181392.1,