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rs145520567

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs145520567(C;T)
Make rs145520567(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position46858411
GeneMYL3
is asnp
is mentioned by
dbSNPrs145520567
dbSNP (old)rs145520567
ClinGenrs145520567
ebirs145520567
HLIrs145520567
Exacrs145520567
Gnomadrs145520567
Varsomers145520567
Maprs145520567
PheGenIrs145520567
Biobankrs145520567
1000 genomesrs145520567
hgdprs145520567
ensemblrs145520567
gopubmedrs145520567
geneviewrs145520567
scholarrs145520567
googlers145520567
pharmgkbrs145520567
gwascentralrs145520567
openSNPrs145520567
23andMers145520567
23andMe allrs145520567
SNP Nexus

SNPshotrs145520567
SNPdbers145520567
MSV3drs145520567
GWAS Ctlgrs145520567
Max Magnitude0
ClinVar
Risk rs145520567(T;T)
Alt rs145520567(T;T)
Reference Rs145520567(C;C)
Significance Probable-Pathogenic
Disease not specified Hypertrophic cardiomyopathy
Variation info
Gene MYL3
CLNDBN not specified Hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000003.11:g.46899901C>T
CLNSRC
CLNACC RCV000036031.4, RCV000262754.1,