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rs727505260

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727505260(-;-)
Make rs727505260(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7577821
GeneDSP
is asnp
is mentioned by
dbSNPrs727505260
ebirs727505260
HLIrs727505260
Exacrs727505260
Varsomers727505260
Maprs727505260
PheGenIrs727505260
hapmaprs727505260
1000 genomesrs727505260
hgdprs727505260
ensemblrs727505260
gopubmedrs727505260
geneviewrs727505260
scholarrs727505260
googlers727505260
pharmgkbrs727505260
gwascentralrs727505260
openSNPrs727505260
23andMers727505260
23andMe allrs727505260
SNP Nexus

SNPshotrs727505260
SNPdbers727505260
MSV3drs727505260
GWAS Ctlgrs727505260
Max Magnitude0
ClinVar
Risk rs727505260(;)
Alt rs727505260(;)
Reference rs727505260(A;A)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSP
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7578054delA
CLNSRC
CLNACC RCV000156783.1,