rs145520567

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs145520567(C;T)

Make rs145520567(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

46858411

Gene

MYL3

is a	snp
is	mentioned by
dbSNP	rs145520567
dbSNP (classic)	rs145520567
ClinGen	rs145520567
ebi	rs145520567
HLI	rs145520567
Exac	rs145520567
Gnomad	rs145520567
Varsome	rs145520567
LitVar	rs145520567
Map	rs145520567
PheGenI	rs145520567
Biobank	rs145520567
1000 genomes	rs145520567
hgdp	rs145520567
ensembl	rs145520567
geneview	rs145520567
scholar	rs145520567
google	rs145520567
pharmgkb	rs145520567
gwascentral	rs145520567
openSNP	rs145520567
23andMe	rs145520567
SNPshot	rs145520567
SNPdbe	rs145520567
MSV3d	rs145520567
GWAS Ctlg	rs145520567

Max Magnitude

0

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,