rs730880742

Orientation

minus

Stabilized

minus

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

Make rs730880742(A;T)

Make rs730880742(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23424984

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880742
dbSNP (classic)	rs730880742
ClinGen	rs730880742
ebi	rs730880742
HLI	rs730880742
Exac	rs730880742
Gnomad	rs730880742
Varsome	rs730880742
LitVar	rs730880742
Map	rs730880742
PheGenI	rs730880742
Biobank	rs730880742
1000 genomes	rs730880742
hgdp	rs730880742
ensembl	rs730880742
geneview	rs730880742
scholar	rs730880742
google	rs730880742
pharmgkb	rs730880742
gwascentral	rs730880742
openSNP	rs730880742
23andMe	rs730880742
SNPshot	rs730880742
SNPdbe	rs730880742
MSV3d	rs730880742
GWAS Ctlg	rs730880742

Max Magnitude

0

ClinVar
Risk	rs730880742(C;C) rs730880742(T;T)
Alt	rs730880742(C;C) rs730880742(T;T)
Reference	Rs730880742(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23894193T>A; NC_000014.8:g.23894193T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000158539.2, RCV000158840.2,