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rs794728121

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728121(A;T)
Make rs794728121(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7580244
GeneDSP
is asnp
is mentioned by
dbSNPrs794728121
ebirs794728121
HLIrs794728121
Exacrs794728121
Varsomers794728121
Maprs794728121
PheGenIrs794728121
hapmaprs794728121
1000 genomesrs794728121
hgdprs794728121
ensemblrs794728121
gopubmedrs794728121
geneviewrs794728121
scholarrs794728121
googlers794728121
pharmgkbrs794728121
gwascentralrs794728121
openSNPrs794728121
23andMers794728121
23andMe allrs794728121
SNP Nexus

SNPshotrs794728121
SNPdbers794728121
MSV3drs794728121
GWAS Ctlgrs794728121
Max Magnitude0
ClinVar
Risk rs794728121(T;T)
Alt rs794728121(T;T)
Reference rs794728121(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7580477A>T
CLNSRC
CLNACC RCV000181318.2,