rs730880866

Orientation

minus

Stabilized

minus

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

Make rs730880866(A;A)

Make rs730880866(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23429778

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880866
dbSNP (classic)	rs730880866
ClinGen	rs730880866
ebi	rs730880866
HLI	rs730880866
Exac	rs730880866
Gnomad	rs730880866
Varsome	rs730880866
LitVar	rs730880866
Map	rs730880866
PheGenI	rs730880866
Biobank	rs730880866
1000 genomes	rs730880866
hgdp	rs730880866
ensembl	rs730880866
geneview	rs730880866
scholar	rs730880866
google	rs730880866
pharmgkb	rs730880866
gwascentral	rs730880866
openSNP	rs730880866
23andMe	rs730880866
SNPshot	rs730880866
SNPdbe	rs730880866
MSV3d	rs730880866
GWAS Ctlg	rs730880866

Max Magnitude

0

ClinVar
Risk	rs730880866(A;A)
Alt	rs730880866(A;A)
Reference	Rs730880866(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23898987C>T
CLNSRC
CLNACC	RCV000158785.1,