rs730880899

Orientation

minus

Stabilized

minus

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

Make rs730880899(C;C)

Make rs730880899(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23424904

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880899
dbSNP (classic)	rs730880899
ClinGen	rs730880899
ebi	rs730880899
HLI	rs730880899
Exac	rs730880899
Gnomad	rs730880899
Varsome	rs730880899
LitVar	rs730880899
Map	rs730880899
PheGenI	rs730880899
Biobank	rs730880899
1000 genomes	rs730880899
hgdp	rs730880899
ensembl	rs730880899
geneview	rs730880899
scholar	rs730880899
google	rs730880899
pharmgkb	rs730880899
gwascentral	rs730880899
openSNP	rs730880899
23andMe	rs730880899
SNPshot	rs730880899
SNPdbe	rs730880899
MSV3d	rs730880899
GWAS Ctlg	rs730880899

Max Magnitude

0

ClinVar
Risk	rs730880899(C;C)
Alt	rs730880899(C;C)
Reference	Rs730880899(G;G)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	MYH7
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23894113C>G
CLNSRC
CLNACC	RCV000221330.1,