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rs794728124

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728124(C;T)
Make rs794728124(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7581402
GeneDSP
is asnp
is mentioned by
dbSNPrs794728124
ebirs794728124
HLIrs794728124
Exacrs794728124
Varsomers794728124
Maprs794728124
PheGenIrs794728124
hapmaprs794728124
1000 genomesrs794728124
hgdprs794728124
ensemblrs794728124
gopubmedrs794728124
geneviewrs794728124
scholarrs794728124
googlers794728124
pharmgkbrs794728124
gwascentralrs794728124
openSNPrs794728124
23andMers794728124
23andMe allrs794728124
SNP Nexus

SNPshotrs794728124
SNPdbers794728124
MSV3drs794728124
GWAS Ctlgrs794728124
Max Magnitude0
ClinVar
Risk rs794728124(T;T)
Alt rs794728124(T;T)
Reference rs794728124(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7581635C>T
CLNSRC
CLNACC RCV000181327.1,