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rs794728137

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794728137(-;-)
Make rs794728137(-;G)
Make rs794728137(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7565509
GeneDSP
is asnp
is mentioned by
dbSNPrs794728137
ebirs794728137
HLIrs794728137
Exacrs794728137
Varsomers794728137
Maprs794728137
PheGenIrs794728137
hapmaprs794728137
1000 genomesrs794728137
hgdprs794728137
ensemblrs794728137
gopubmedrs794728137
geneviewrs794728137
scholarrs794728137
googlers794728137
pharmgkbrs794728137
gwascentralrs794728137
openSNPrs794728137
23andMers794728137
23andMe allrs794728137
SNP Nexus

SNPshotrs794728137
SNPdbers794728137
MSV3drs794728137
GWAS Ctlgrs794728137
Max Magnitude0
ClinVar
Risk rs794728137(G;G)
Alt rs794728137(G;G)
Reference rs794728137(;)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7565742dupG
CLNSRC
CLNACC RCV000181358.1,