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rs794728159

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728159(-;-)
Make rs794728159(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7585418
GeneDSP
is asnp
is mentioned by
dbSNPrs794728159
ebirs794728159
HLIrs794728159
Exacrs794728159
Varsomers794728159
Maprs794728159
PheGenIrs794728159
hapmaprs794728159
1000 genomesrs794728159
hgdprs794728159
ensemblrs794728159
gopubmedrs794728159
geneviewrs794728159
scholarrs794728159
googlers794728159
pharmgkbrs794728159
gwascentralrs794728159
openSNPrs794728159
23andMers794728159
23andMe allrs794728159
SNP Nexus

SNPshotrs794728159
SNPdbers794728159
MSV3drs794728159
GWAS Ctlgrs794728159
Max Magnitude0
ClinVar
Risk rs794728159(;)
Alt rs794728159(;)
Reference rs794728159(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7585651delC
CLNSRC
CLNACC RCV000181394.1,