rs730880835

Orientation

minus

Stabilized

minus

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

Make rs730880835(A;C)

Make rs730880835(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23432704

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880835
dbSNP (classic)	rs730880835
ClinGen	rs730880835
ebi	rs730880835
HLI	rs730880835
Exac	rs730880835
Gnomad	rs730880835
Varsome	rs730880835
LitVar	rs730880835
Map	rs730880835
PheGenI	rs730880835
Biobank	rs730880835
1000 genomes	rs730880835
hgdp	rs730880835
ensembl	rs730880835
geneview	rs730880835
scholar	rs730880835
google	rs730880835
pharmgkb	rs730880835
gwascentral	rs730880835
openSNP	rs730880835
23andMe	rs730880835
SNPshot	rs730880835
SNPdbe	rs730880835
MSV3d	rs730880835
GWAS Ctlg	rs730880835

Max Magnitude

0

ClinVar
Risk	rs730880835(C;C) rs730880835(T;T)
Alt	rs730880835(C;C) rs730880835(T;T)
Reference	Rs730880835(A;A)
Significance	Pathogenic
Disease	not specified
Variation	info
Gene	MYH7
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23901913T>A
CLNSRC	Children's Hospital of Eastern Ontario
CLNACC	RCV000168836.2,