rs730880764

Orientation

minus

Stabilized

minus

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

Make rs730880764(A;A)

Make rs730880764(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23423609

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880764
dbSNP (classic)	rs730880764
ClinGen	rs730880764
ebi	rs730880764
HLI	rs730880764
Exac	rs730880764
Gnomad	rs730880764
Varsome	rs730880764
LitVar	rs730880764
Map	rs730880764
PheGenI	rs730880764
Biobank	rs730880764
1000 genomes	rs730880764
hgdp	rs730880764
ensembl	rs730880764
geneview	rs730880764
scholar	rs730880764
google	rs730880764
pharmgkb	rs730880764
gwascentral	rs730880764
openSNP	rs730880764
23andMe	rs730880764
SNPshot	rs730880764
SNPdbe	rs730880764
MSV3d	rs730880764
GWAS Ctlg	rs730880764

Max Magnitude

0

ClinVar
Risk	rs730880764(A;A)
Alt	rs730880764(A;A)
Reference	Rs730880764(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23892818C>T
CLNSRC
CLNACC	RCV000158584.1,