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rs794728135

From SNPedia

Orientationplus
Geno Mag Summary
(GCTTGATGC;GCTTGATGC) 0 common in clinvar
Make rs794728135(-;-)
Make rs794728135(-;CTTGATGCG)
Make rs794728135(CTTGATGCG;CTTGATGCG)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7555790
GeneDSP
is asnp
is mentioned by
dbSNPrs794728135
ClinGenrs794728135
ebirs794728135
HLIrs794728135
Exacrs794728135
Varsomers794728135
Maprs794728135
PheGenIrs794728135
hapmaprs794728135
1000 genomesrs794728135
hgdprs794728135
ensemblrs794728135
gopubmedrs794728135
geneviewrs794728135
scholarrs794728135
googlers794728135
pharmgkbrs794728135
gwascentralrs794728135
openSNPrs794728135
23andMers794728135
23andMe allrs794728135
SNP Nexus

SNPshotrs794728135
SNPdbers794728135
MSV3drs794728135
GWAS Ctlgrs794728135
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs794728135(GCTTGATGC;GCTTGATGC)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7556023_7556031delCTTGATGCG
CLNSRC
CLNACC RCV000181356.2,