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rs794728143

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728143(-;-)
Make rs794728143(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7584199
GeneDSP
is asnp
is mentioned by
dbSNPrs794728143
ebirs794728143
HLIrs794728143
Exacrs794728143
Varsomers794728143
Maprs794728143
PheGenIrs794728143
hapmaprs794728143
1000 genomesrs794728143
hgdprs794728143
ensemblrs794728143
gopubmedrs794728143
geneviewrs794728143
scholarrs794728143
googlers794728143
pharmgkbrs794728143
gwascentralrs794728143
openSNPrs794728143
23andMers794728143
23andMe allrs794728143
SNP Nexus

SNPshotrs794728143
SNPdbers794728143
MSV3drs794728143
GWAS Ctlgrs794728143
Max Magnitude0
ClinVar
Risk rs794728143(;)
Alt rs794728143(;)
Reference rs794728143(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7584432delG
CLNSRC
CLNACC RCV000181366.1,