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rs794728130

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728130(C;T)
Make rs794728130(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7584112
GeneDSP
is asnp
is mentioned by
dbSNPrs794728130
ebirs794728130
HLIrs794728130
Exacrs794728130
Varsomers794728130
Maprs794728130
PheGenIrs794728130
hapmaprs794728130
1000 genomesrs794728130
hgdprs794728130
ensemblrs794728130
gopubmedrs794728130
geneviewrs794728130
scholarrs794728130
googlers794728130
pharmgkbrs794728130
gwascentralrs794728130
openSNPrs794728130
23andMers794728130
23andMe allrs794728130
SNP Nexus

SNPshotrs794728130
SNPdbers794728130
MSV3drs794728130
GWAS Ctlgrs794728130
Max Magnitude0
ClinVar
Risk rs794728130(T;T)
Alt rs794728130(T;T)
Reference rs794728130(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7584345C>T
CLNSRC
CLNACC RCV000181344.2,