rs730880804

Orientation

minus

Stabilized

minus

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

Make rs730880804(A;C)

Make rs730880804(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23416869

Gene	MHRT, MYH7

is a	snp
is	mentioned by
dbSNP	rs730880804
dbSNP (classic)	rs730880804
ClinGen	rs730880804
ebi	rs730880804
HLI	rs730880804
Exac	rs730880804
Gnomad	rs730880804
Varsome	rs730880804
LitVar	rs730880804
Map	rs730880804
PheGenI	rs730880804
Biobank	rs730880804
1000 genomes	rs730880804
hgdp	rs730880804
ensembl	rs730880804
geneview	rs730880804
scholar	rs730880804
google	rs730880804
pharmgkb	rs730880804
gwascentral	rs730880804
openSNP	rs730880804
23andMe	rs730880804
SNPshot	rs730880804
SNPdbe	rs730880804
MSV3d	rs730880804
GWAS Ctlg	rs730880804

Max Magnitude

0

ClinVar
Risk	rs730880804(C;C)
Alt	rs730880804(C;C)
Reference	Rs730880804(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7 MHRT
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23886078T>G
CLNSRC
CLNACC	RCV000158664.1,