rs730880859

Orientation

minus

Stabilized

minus

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

Make rs730880859(A;A)

Make rs730880859(A;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23430595

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880859
dbSNP (classic)	rs730880859
ClinGen	rs730880859
ebi	rs730880859
HLI	rs730880859
Exac	rs730880859
Gnomad	rs730880859
Varsome	rs730880859
LitVar	rs730880859
Map	rs730880859
PheGenI	rs730880859
Biobank	rs730880859
1000 genomes	rs730880859
hgdp	rs730880859
ensembl	rs730880859
geneview	rs730880859
scholar	rs730880859
google	rs730880859
pharmgkb	rs730880859
gwascentral	rs730880859
openSNP	rs730880859
23andMe	rs730880859
SNPshot	rs730880859
SNPdbe	rs730880859
MSV3d	rs730880859
GWAS Ctlg	rs730880859

Max Magnitude

0

ClinVar
Risk	rs730880859(A;A)
Alt	rs730880859(A;A)
Reference	Rs730880859(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23899804A>T
CLNSRC
CLNACC	RCV000158773.1,