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rs794728140

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728140(-;-)
Make rs794728140(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7579609
GeneDSP
is asnp
is mentioned by
dbSNPrs794728140
ebirs794728140
HLIrs794728140
Exacrs794728140
Varsomers794728140
Maprs794728140
PheGenIrs794728140
hapmaprs794728140
1000 genomesrs794728140
hgdprs794728140
ensemblrs794728140
gopubmedrs794728140
geneviewrs794728140
scholarrs794728140
googlers794728140
pharmgkbrs794728140
gwascentralrs794728140
openSNPrs794728140
23andMers794728140
23andMe allrs794728140
SNP Nexus

SNPshotrs794728140
SNPdbers794728140
MSV3drs794728140
GWAS Ctlgrs794728140
Max Magnitude0
ClinVar
Risk rs794728140(;)
Alt rs794728140(;)
Reference rs794728140(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7579842delA
CLNSRC
CLNACC RCV000181363.1,