rs730880759

Orientation

minus

Stabilized

minus

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

Make rs730880759(A;A)

Make rs730880759(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23424068

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880759
dbSNP (classic)	rs730880759
ClinGen	rs730880759
ebi	rs730880759
HLI	rs730880759
Exac	rs730880759
Gnomad	rs730880759
Varsome	rs730880759
LitVar	rs730880759
Map	rs730880759
PheGenI	rs730880759
Biobank	rs730880759
1000 genomes	rs730880759
hgdp	rs730880759
ensembl	rs730880759
geneview	rs730880759
scholar	rs730880759
google	rs730880759
pharmgkb	rs730880759
gwascentral	rs730880759
openSNP	rs730880759
23andMe	rs730880759
SNPshot	rs730880759
SNPdbe	rs730880759
MSV3d	rs730880759
GWAS Ctlg	rs730880759

Max Magnitude

0

ClinVar
Risk	rs730880759(A;A) rs730880759(T;T)
Alt	rs730880759(A;A) rs730880759(T;T)
Reference	Rs730880759(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23893277C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000158572.2,