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

rs794728149

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794728149(-;-)
Make rs794728149(-;A)
Make rs794728149(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7585135
GeneDSP
is asnp
is mentioned by
dbSNPrs794728149
ebirs794728149
HLIrs794728149
Exacrs794728149
Varsomers794728149
Maprs794728149
PheGenIrs794728149
hapmaprs794728149
1000 genomesrs794728149
hgdprs794728149
ensemblrs794728149
gopubmedrs794728149
geneviewrs794728149
scholarrs794728149
googlers794728149
pharmgkbrs794728149
gwascentralrs794728149
openSNPrs794728149
23andMers794728149
23andMe allrs794728149
SNP Nexus

SNPshotrs794728149
SNPdbers794728149
MSV3drs794728149
GWAS Ctlgrs794728149
Max Magnitude0
ClinVar
Risk rs794728149(A;A)
Alt rs794728149(A;A)
Reference rs794728149(;)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7585368dupA
CLNSRC
CLNACC RCV000181372.1,