rs730880961

Orientation

minus

Stabilized

minus

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

Make rs730880961(C;T)

Make rs730880961(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

46860703

Gene

MYL3

is a	snp
is	mentioned by
dbSNP	rs730880961
dbSNP (classic)	rs730880961
ClinGen	rs730880961
ebi	rs730880961
HLI	rs730880961
Exac	rs730880961
Gnomad	rs730880961
Varsome	rs730880961
LitVar	rs730880961
Map	rs730880961
PheGenI	rs730880961
Biobank	rs730880961
1000 genomes	rs730880961
hgdp	rs730880961
ensembl	rs730880961
geneview	rs730880961
scholar	rs730880961
google	rs730880961
pharmgkb	rs730880961
gwascentral	rs730880961
openSNP	rs730880961
23andMe	rs730880961
SNPshot	rs730880961
SNPdbe	rs730880961
MSV3d	rs730880961
GWAS Ctlg	rs730880961

Max Magnitude

0

ClinVar
Risk	rs730880961(A;A) rs730880961(T;T)
Alt	rs730880961(A;A) rs730880961(T;T)
Reference	Rs730880961(C;C)
Significance	Pathogenic
Disease	not specified Hypertrophic cardiomyopathy
Variation	info
Gene	MYL3
CLNDBN	not specified Hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000003.11:g.46902193G>A; NC_000003.11:g.46902193G>T
CLNSRC
CLNACC	RCV000158961.2, RCV000233649.1, RCV000459761.1,