Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728142

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728142(-;-)
Make rs794728142(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7579923
GeneDSP
is asnp
is mentioned by
dbSNPrs794728142
ebirs794728142
HLIrs794728142
Exacrs794728142
Varsomers794728142
Maprs794728142
PheGenIrs794728142
hapmaprs794728142
1000 genomesrs794728142
hgdprs794728142
ensemblrs794728142
gopubmedrs794728142
geneviewrs794728142
scholarrs794728142
googlers794728142
pharmgkbrs794728142
gwascentralrs794728142
openSNPrs794728142
23andMers794728142
23andMe allrs794728142
SNP Nexus

SNPshotrs794728142
SNPdbers794728142
MSV3drs794728142
GWAS Ctlgrs794728142
Max Magnitude0
ClinVar
Risk rs794728142(;)
Alt rs794728142(;)
Reference rs794728142(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7580156delG
CLNSRC
CLNACC RCV000181365.2,