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rs794728118

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728118(C;T)
Make rs794728118(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7575475
GeneDSP
is asnp
is mentioned by
dbSNPrs794728118
ebirs794728118
HLIrs794728118
Exacrs794728118
Varsomers794728118
Maprs794728118
PheGenIrs794728118
hapmaprs794728118
1000 genomesrs794728118
hgdprs794728118
ensemblrs794728118
gopubmedrs794728118
geneviewrs794728118
scholarrs794728118
googlers794728118
pharmgkbrs794728118
gwascentralrs794728118
openSNPrs794728118
23andMers794728118
23andMe allrs794728118
SNP Nexus

SNPshotrs794728118
SNPdbers794728118
MSV3drs794728118
GWAS Ctlgrs794728118
Max Magnitude0
ClinVar
Risk rs794728118(T;T)
Alt rs794728118(T;T)
Reference rs794728118(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7575708C>T
CLNSRC
CLNACC RCV000181302.1,