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rs794728141

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794728141(-;-)
Make rs794728141(-;G)
Make rs794728141(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7579616
GeneDSP
is asnp
is mentioned by
dbSNPrs794728141
ebirs794728141
HLIrs794728141
Exacrs794728141
Varsomers794728141
Maprs794728141
PheGenIrs794728141
hapmaprs794728141
1000 genomesrs794728141
hgdprs794728141
ensemblrs794728141
gopubmedrs794728141
geneviewrs794728141
scholarrs794728141
googlers794728141
pharmgkbrs794728141
gwascentralrs794728141
openSNPrs794728141
23andMers794728141
23andMe allrs794728141
SNP Nexus

SNPshotrs794728141
SNPdbers794728141
MSV3drs794728141
GWAS Ctlgrs794728141
Max Magnitude0
ClinVar
Risk rs794728141(G;G)
Alt rs794728141(G;G)
Reference rs794728141(;)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7579849dupG
CLNSRC
CLNACC RCV000181364.1,