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rs794728114

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728114(A;A)
Make rs794728114(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7570473
GeneDSP
is asnp
is mentioned by
dbSNPrs794728114
ebirs794728114
HLIrs794728114
Exacrs794728114
Varsomers794728114
Maprs794728114
PheGenIrs794728114
hapmaprs794728114
1000 genomesrs794728114
hgdprs794728114
ensemblrs794728114
gopubmedrs794728114
geneviewrs794728114
scholarrs794728114
googlers794728114
pharmgkbrs794728114
gwascentralrs794728114
openSNPrs794728114
23andMers794728114
23andMe allrs794728114
SNP Nexus

SNPshotrs794728114
SNPdbers794728114
MSV3drs794728114
GWAS Ctlgrs794728114
Max Magnitude0
ClinVar
Risk rs794728114(A;A)
Alt rs794728114(A;A)
Reference rs794728114(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7570706G>A
CLNSRC
CLNACC RCV000181292.1,