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rs794728111

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728111(A;G)
Make rs794728111(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7567779
GeneDSP
is asnp
is mentioned by
dbSNPrs794728111
ebirs794728111
HLIrs794728111
Exacrs794728111
Varsomers794728111
Maprs794728111
PheGenIrs794728111
hapmaprs794728111
1000 genomesrs794728111
hgdprs794728111
ensemblrs794728111
gopubmedrs794728111
geneviewrs794728111
scholarrs794728111
googlers794728111
pharmgkbrs794728111
gwascentralrs794728111
openSNPrs794728111
23andMers794728111
23andMe allrs794728111
SNP Nexus

SNPshotrs794728111
SNPdbers794728111
MSV3drs794728111
GWAS Ctlgrs794728111
Max Magnitude0
ClinVar
Risk rs794728111(G;G)
Alt rs794728111(G;G)
Reference rs794728111(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7568012A>G
CLNSRC
CLNACC RCV000181281.1,