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rs727504498

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504498(C;T)
Make rs727504498(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7570477
GeneDSP
is asnp
is mentioned by
dbSNPrs727504498
ebirs727504498
HLIrs727504498
Exacrs727504498
Varsomers727504498
Maprs727504498
PheGenIrs727504498
hapmaprs727504498
1000 genomesrs727504498
hgdprs727504498
ensemblrs727504498
gopubmedrs727504498
geneviewrs727504498
scholarrs727504498
googlers727504498
pharmgkbrs727504498
gwascentralrs727504498
openSNPrs727504498
23andMers727504498
23andMe allrs727504498
SNP Nexus

SNPshotrs727504498
SNPdbers727504498
MSV3drs727504498
GWAS Ctlgrs727504498
Max Magnitude0
ClinVar
Risk rs727504498(T;T)
Alt rs727504498(T;T)
Reference rs727504498(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene DSP
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7570710C>T
CLNSRC
CLNACC RCV000155634.1,