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rs727503001

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727503001(A;A)
Make rs727503001(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7579820
GeneDSP
is asnp
is mentioned by
dbSNPrs727503001
ebirs727503001
HLIrs727503001
Exacrs727503001
Varsomers727503001
Maprs727503001
PheGenIrs727503001
hapmaprs727503001
1000 genomesrs727503001
hgdprs727503001
ensemblrs727503001
gopubmedrs727503001
geneviewrs727503001
scholarrs727503001
googlers727503001
pharmgkbrs727503001
gwascentralrs727503001
openSNPrs727503001
23andMers727503001
23andMe allrs727503001
SNP Nexus

SNPshotrs727503001
SNPdbers727503001
MSV3drs727503001
GWAS Ctlgrs727503001
Max Magnitude0
ClinVar
Risk rs727503001(A;A)
Alt rs727503001(A;A)
Reference rs727503001(T;T)
Significance Pathogenic
Disease Cardiomyopathy not provided
Variation info
Gene DSP
CLNDBN Cardiomyopathy not provided
Reversed 0
HGVS NC_000006.11:g.7580053T>A
CLNSRC
CLNACC RCV000150567.1, RCV000181312.2,