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rs794728136

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728136(-;-)
Make rs794728136(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7555820
GeneDSP
is asnp
is mentioned by
dbSNPrs794728136
ebirs794728136
HLIrs794728136
Exacrs794728136
Varsomers794728136
Maprs794728136
PheGenIrs794728136
hapmaprs794728136
1000 genomesrs794728136
hgdprs794728136
ensemblrs794728136
gopubmedrs794728136
geneviewrs794728136
scholarrs794728136
googlers794728136
pharmgkbrs794728136
gwascentralrs794728136
openSNPrs794728136
23andMers794728136
23andMe allrs794728136
SNP Nexus

SNPshotrs794728136
SNPdbers794728136
MSV3drs794728136
GWAS Ctlgrs794728136
Max Magnitude0
ClinVar
Risk rs794728136(;)
Alt rs794728136(;)
Reference rs794728136(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7556053delT
CLNSRC
CLNACC RCV000181357.1,