Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728112

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728112(A;T)
Make rs794728112(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7567411
GeneDSP
is asnp
is mentioned by
dbSNPrs794728112
ebirs794728112
HLIrs794728112
Exacrs794728112
Varsomers794728112
Maprs794728112
PheGenIrs794728112
hapmaprs794728112
1000 genomesrs794728112
hgdprs794728112
ensemblrs794728112
gopubmedrs794728112
geneviewrs794728112
scholarrs794728112
googlers794728112
pharmgkbrs794728112
gwascentralrs794728112
openSNPrs794728112
23andMers794728112
23andMe allrs794728112
SNP Nexus

SNPshotrs794728112
SNPdbers794728112
MSV3drs794728112
GWAS Ctlgrs794728112
Max Magnitude0
ClinVar
Risk rs794728112(T;T)
Alt rs794728112(T;T)
Reference rs794728112(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene DSP
CLNDBN not specified
Reversed 0
HGVS NC_000006.11:g.7567644A>T
CLNSRC
CLNACC RCV000181286.1,