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rs794728147

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794728147(-;-)
Make rs794728147(-;G)
Make rs794728147(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7583660
GeneDSP
is asnp
is mentioned by
dbSNPrs794728147
ebirs794728147
HLIrs794728147
Exacrs794728147
Varsomers794728147
Maprs794728147
PheGenIrs794728147
hapmaprs794728147
1000 genomesrs794728147
hgdprs794728147
ensemblrs794728147
gopubmedrs794728147
geneviewrs794728147
scholarrs794728147
googlers794728147
pharmgkbrs794728147
gwascentralrs794728147
openSNPrs794728147
23andMers794728147
23andMe allrs794728147
SNP Nexus

SNPshotrs794728147
SNPdbers794728147
MSV3drs794728147
GWAS Ctlgrs794728147
Max Magnitude0
ClinVar
Risk rs794728147(G;G)
Alt rs794728147(G;G)
Reference rs794728147(;)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7583893dupG
CLNSRC
CLNACC RCV000181370.1,