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rs794728144

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794728144(-;-)
Make rs794728144(-;AAATCGA)
Make rs794728144(AAATCGA;AAATCGA)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7579931
GeneDSP
is asnp
is mentioned by
dbSNPrs794728144
ebirs794728144
HLIrs794728144
Exacrs794728144
Varsomers794728144
Maprs794728144
PheGenIrs794728144
hapmaprs794728144
1000 genomesrs794728144
hgdprs794728144
ensemblrs794728144
gopubmedrs794728144
geneviewrs794728144
scholarrs794728144
googlers794728144
pharmgkbrs794728144
gwascentralrs794728144
openSNPrs794728144
23andMers794728144
23andMe allrs794728144
SNP Nexus

SNPshotrs794728144
SNPdbers794728144
MSV3drs794728144
GWAS Ctlgrs794728144
Max Magnitude0
ClinVar
Risk rs794728144(GAAAATC;GAAAATC)
Alt rs794728144(GAAAATC;GAAAATC)
Reference rs794728144(;)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7580158_7580164dupAAATCGA
CLNSRC
CLNACC RCV000181367.1,