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rs794728156

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728156(C;T)
Make rs794728156(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7542066
GeneDSP, LOC101928076
is asnp
is mentioned by
dbSNPrs794728156
ebirs794728156
HLIrs794728156
Exacrs794728156
Varsomers794728156
Maprs794728156
PheGenIrs794728156
hapmaprs794728156
1000 genomesrs794728156
hgdprs794728156
ensemblrs794728156
gopubmedrs794728156
geneviewrs794728156
scholarrs794728156
googlers794728156
pharmgkbrs794728156
gwascentralrs794728156
openSNPrs794728156
23andMers794728156
23andMe allrs794728156
SNP Nexus

SNPshotrs794728156
SNPdbers794728156
MSV3drs794728156
GWAS Ctlgrs794728156
Max Magnitude0
ClinVar
Risk rs794728156(T;T)
Alt rs794728156(T;T)
Reference rs794728156(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP LOC101928076
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7542299C>T
CLNSRC
CLNACC RCV000181391.1,