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rs794728145

From SNPedia

Orientationplus
Geno Mag Summary
(ACAGCGCC;ACAGCGCC) 0 common in clinvar
Make rs794728145(ACAGCGCC;GTG)
Make rs794728145(GTG;GTG)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7582812
GeneDSP
is asnp
is mentioned by
dbSNPrs794728145
ebirs794728145
HLIrs794728145
Exacrs794728145
Varsomers794728145
Maprs794728145
PheGenIrs794728145
hapmaprs794728145
1000 genomesrs794728145
hgdprs794728145
ensemblrs794728145
gopubmedrs794728145
geneviewrs794728145
scholarrs794728145
googlers794728145
pharmgkbrs794728145
gwascentralrs794728145
openSNPrs794728145
23andMers794728145
23andMe allrs794728145
SNP Nexus

SNPshotrs794728145
SNPdbers794728145
MSV3drs794728145
GWAS Ctlgrs794728145
Max Magnitude0
ClinVar
Risk rs794728145(GTG;GTG)
Alt rs794728145(GTG;GTG)
Reference rs794728145(ACAGCGCC;ACAGCGCC)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7583045_7583052delACAGCGCCinsGTG
CLNSRC
CLNACC RCV000181368.1,