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rs794728148

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794728148(-;-)
Make rs794728148(-;CT)
Make rs794728148(CT;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7583772
GeneDSP
is asnp
is mentioned by
dbSNPrs794728148
ebirs794728148
HLIrs794728148
Exacrs794728148
Varsomers794728148
Maprs794728148
PheGenIrs794728148
hapmaprs794728148
1000 genomesrs794728148
hgdprs794728148
ensemblrs794728148
gopubmedrs794728148
geneviewrs794728148
scholarrs794728148
googlers794728148
pharmgkbrs794728148
gwascentralrs794728148
openSNPrs794728148
23andMers794728148
23andMe allrs794728148
SNP Nexus

SNPshotrs794728148
SNPdbers794728148
MSV3drs794728148
GWAS Ctlgrs794728148
Max Magnitude0
ClinVar
Risk rs794728148(CT;CT)
Alt rs794728148(CT;CT)
Reference rs794728148(;)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7584005_7584006insCT
CLNSRC
CLNACC RCV000181371.1,