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rs794728131

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728131(C;C)
Make rs794728131(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7584169
GeneDSP
is asnp
is mentioned by
dbSNPrs794728131
ebirs794728131
HLIrs794728131
Exacrs794728131
Varsomers794728131
Maprs794728131
PheGenIrs794728131
hapmaprs794728131
1000 genomesrs794728131
hgdprs794728131
ensemblrs794728131
gopubmedrs794728131
geneviewrs794728131
scholarrs794728131
googlers794728131
pharmgkbrs794728131
gwascentralrs794728131
openSNPrs794728131
23andMers794728131
23andMe allrs794728131
SNP Nexus

SNPshotrs794728131
SNPdbers794728131
MSV3drs794728131
GWAS Ctlgrs794728131
Max Magnitude0
ClinVar
Risk rs794728131(C;C)
Alt rs794728131(C;C)
Reference rs794728131(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7584402G>C
CLNSRC
CLNACC RCV000181345.1,