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rs794728093

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTTGAAGGGATG;CTTGAAGGGATG) 0 common in clinvar
(GCTTGAAGGGAT;GCTTGAAGGGAT) 0 common in clinvar
Make rs794728093(-;-)
Make rs794728093(-;CTTGAAGGGATG)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31524703
GeneDSG2
is asnp
is mentioned by
dbSNPrs794728093
dbSNP (old)rs794728093
ClinGenrs794728093
ebirs794728093
HLIrs794728093
Exacrs794728093
Varsomers794728093
Maprs794728093
PheGenIrs794728093
Biobankrs794728093
1000 genomesrs794728093
hgdprs794728093
ensemblrs794728093
gopubmedrs794728093
geneviewrs794728093
scholarrs794728093
googlers794728093
pharmgkbrs794728093
gwascentralrs794728093
openSNPrs794728093
23andMers794728093
23andMe allrs794728093
SNP Nexus

SNPshotrs794728093
SNPdbers794728093
MSV3drs794728093
GWAS Ctlgrs794728093
Max Magnitude0
ClinVar
Risk rs794728093(-;-) Rs794728093(GCTTGAAGGGAT;GCTTGAAGGGAT)
Alt rs794728093(-;-) Rs794728093(GCTTGAAGGGAT;GCTTGAAGGGAT)
Reference Rs794728093(CTTGAAGGGATG;CTTGAAGGGATG)
Significance Pathogenic
Disease not provided
Variation info
Gene DSG2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.29104666_29104677delCTTGAAGGGATG
CLNSRC
CLNACC RCV000181240.2,