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rs794728139

From SNPedia

Orientationplus
Geno Mag Summary
(CAATT;CAATT) 0 common in clinvar
Make rs794728139(-;-)
Make rs794728139(-;CAATT)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7577035
GeneDSP
is asnp
is mentioned by
dbSNPrs794728139
ebirs794728139
HLIrs794728139
Exacrs794728139
Varsomers794728139
Maprs794728139
PheGenIrs794728139
hapmaprs794728139
1000 genomesrs794728139
hgdprs794728139
ensemblrs794728139
gopubmedrs794728139
geneviewrs794728139
scholarrs794728139
googlers794728139
pharmgkbrs794728139
gwascentralrs794728139
openSNPrs794728139
23andMers794728139
23andMe allrs794728139
SNP Nexus

SNPshotrs794728139
SNPdbers794728139
MSV3drs794728139
GWAS Ctlgrs794728139
Max Magnitude0
ClinVar
Risk rs794728139(;)
Alt rs794728139(;)
Reference rs794728139(CAATT;CAATT)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7577268_7577272delCAATT
CLNSRC
CLNACC RCV000181362.2,