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rs794728150

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794728150(-;-)
Make rs794728150(-;G)
Make rs794728150(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7585444
GeneDSP
is asnp
is mentioned by
dbSNPrs794728150
ebirs794728150
HLIrs794728150
Exacrs794728150
Varsomers794728150
Maprs794728150
PheGenIrs794728150
hapmaprs794728150
1000 genomesrs794728150
hgdprs794728150
ensemblrs794728150
gopubmedrs794728150
geneviewrs794728150
scholarrs794728150
googlers794728150
pharmgkbrs794728150
gwascentralrs794728150
openSNPrs794728150
23andMers794728150
23andMe allrs794728150
SNP Nexus

SNPshotrs794728150
SNPdbers794728150
MSV3drs794728150
GWAS Ctlgrs794728150
Max Magnitude0
ClinVar
Risk rs794728150(G;G)
Alt rs794728150(G;G)
Reference rs794728150(;)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7585677dupG
CLNSRC
CLNACC RCV000181373.1,