rs730880839

Orientation

minus

Stabilized

minus

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

Make rs730880839(A;G)

Make rs730880839(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23432648

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880839
dbSNP (classic)	rs730880839
ClinGen	rs730880839
ebi	rs730880839
HLI	rs730880839
Exac	rs730880839
Gnomad	rs730880839
Varsome	rs730880839
LitVar	rs730880839
Map	rs730880839
PheGenI	rs730880839
Biobank	rs730880839
1000 genomes	rs730880839
hgdp	rs730880839
ensembl	rs730880839
geneview	rs730880839
scholar	rs730880839
google	rs730880839
pharmgkb	rs730880839
gwascentral	rs730880839
openSNP	rs730880839
23andMe	rs730880839
SNPshot	rs730880839
SNPdbe	rs730880839
MSV3d	rs730880839
GWAS Ctlg	rs730880839

Max Magnitude

0

ClinVar
Risk	rs730880839(G;G)
Alt	rs730880839(G;G)
Reference	Rs730880839(A;A)
Significance	Probable-Pathogenic
Disease	not provided not specified
Variation	info
Gene	MYH7
CLNDBN	not provided not specified
Reversed	1
HGVS	NC_000014.8:g.23901857T>C
CLNSRC
CLNACC	RCV000158737.2, RCV000223786.1,