rs730880807

Orientation

minus

Stabilized

minus

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

Make rs730880807(A;A)

Make rs730880807(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23416248

Gene	MHRT, MYH7

is a	snp
is	mentioned by
dbSNP	rs730880807
dbSNP (classic)	rs730880807
ClinGen	rs730880807
ebi	rs730880807
HLI	rs730880807
Exac	rs730880807
Gnomad	rs730880807
Varsome	rs730880807
LitVar	rs730880807
Map	rs730880807
PheGenI	rs730880807
Biobank	rs730880807
1000 genomes	rs730880807
hgdp	rs730880807
ensembl	rs730880807
geneview	rs730880807
scholar	rs730880807
google	rs730880807
pharmgkb	rs730880807
gwascentral	rs730880807
openSNP	rs730880807
23andMe	rs730880807
SNPshot	rs730880807
SNPdbe	rs730880807
MSV3d	rs730880807
GWAS Ctlg	rs730880807

Max Magnitude

0

ClinVar
Risk	rs730880807(A;A)
Alt	rs730880807(A;A)
Reference	Rs730880807(C;C)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	MYH7 MHRT
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23885457G>T
CLNSRC
CLNACC	RCV000158668.2,