rs730880756

Orientation

minus

Stabilized

minus

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

Make rs730880756(A;A)

Make rs730880756(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23424122

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880756
dbSNP (classic)	rs730880756
ClinGen	rs730880756
ebi	rs730880756
HLI	rs730880756
Exac	rs730880756
Gnomad	rs730880756
Varsome	rs730880756
LitVar	rs730880756
Map	rs730880756
PheGenI	rs730880756
Biobank	rs730880756
1000 genomes	rs730880756
hgdp	rs730880756
ensembl	rs730880756
geneview	rs730880756
scholar	rs730880756
google	rs730880756
pharmgkb	rs730880756
gwascentral	rs730880756
openSNP	rs730880756
23andMe	rs730880756
SNPshot	rs730880756
SNPdbe	rs730880756
MSV3d	rs730880756
GWAS Ctlg	rs730880756

Max Magnitude

0

ClinVar
Risk	rs730880756(A;A)
Alt	rs730880756(A;A)
Reference	Rs730880756(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23893331C>T
CLNSRC
CLNACC	RCV000158564.1,