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rs794728146

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728146(-;-)
Make rs794728146(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7583535
GeneDSP
is asnp
is mentioned by
dbSNPrs794728146
ebirs794728146
HLIrs794728146
Exacrs794728146
Varsomers794728146
Maprs794728146
PheGenIrs794728146
hapmaprs794728146
1000 genomesrs794728146
hgdprs794728146
ensemblrs794728146
gopubmedrs794728146
geneviewrs794728146
scholarrs794728146
googlers794728146
pharmgkbrs794728146
gwascentralrs794728146
openSNPrs794728146
23andMers794728146
23andMe allrs794728146
SNP Nexus

SNPshotrs794728146
SNPdbers794728146
MSV3drs794728146
GWAS Ctlgrs794728146
Max Magnitude0
ClinVar
Risk rs794728146(;)
Alt rs794728146(;)
Reference rs794728146(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7583768delA
CLNSRC
CLNACC RCV000181369.1,