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rs727502993

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs727502993(-;-)
Make rs727502993(-;AC)
Make rs727502993(AC;AC)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7555756
GeneDSP
is asnp
is mentioned by
dbSNPrs727502993
ebirs727502993
HLIrs727502993
Exacrs727502993
Varsomers727502993
Maprs727502993
PheGenIrs727502993
hapmaprs727502993
1000 genomesrs727502993
hgdprs727502993
ensemblrs727502993
gopubmedrs727502993
geneviewrs727502993
scholarrs727502993
googlers727502993
pharmgkbrs727502993
gwascentralrs727502993
openSNPrs727502993
23andMers727502993
23andMe allrs727502993
SNP Nexus

SNPshotrs727502993
SNPdbers727502993
MSV3drs727502993
GWAS Ctlgrs727502993
Max Magnitude0
ClinVar
Risk rs727502993(AC;AC)
Alt rs727502993(AC;AC)
Reference rs727502993(;)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSP
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7555988_7555989dupAC
CLNSRC
CLNACC RCV000150551.1,