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rs185821167

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs185821167(A;A)
Make rs185821167(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31524749
GeneDSG2
is asnp
is mentioned by
dbSNPrs185821167
ebirs185821167
HLIrs185821167
Exacrs185821167
Varsomers185821167
Maprs185821167
PheGenIrs185821167
hapmaprs185821167
1000 genomesrs185821167
hgdprs185821167
ensemblrs185821167
gopubmedrs185821167
geneviewrs185821167
scholarrs185821167
googlers185821167
pharmgkbrs185821167
gwascentralrs185821167
openSNPrs185821167
23andMers185821167
23andMe allrs185821167
SNP Nexus

SNPshotrs185821167
SNPdbers185821167
MSV3drs185821167
GWAS Ctlgrs185821167
Max Magnitude0
ClinVar
Risk rs185821167(A;A)
Alt rs185821167(A;A)
Reference rs185821167(G;G)
Significance Probable-Pathogenic
Disease not specified Arrhythmogenic right ventricular cardiomyopathy not provided
Variation info
Gene DSG2
CLNDBN not specified Arrhythmogenic right ventricular cardiomyopathy, type 10 not provided
Reversed 0
HGVS NC_000018.9:g.29104712G>A; NC_000018.9:g.29104712G>T
CLNSRC
CLNACC RCV000037318.3, RCV000205277.1, RCV000181210.1,