rs730880822

Orientation

minus

Stabilized

minus

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

Make rs730880822(A;A)

Make rs730880822(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23415020

Gene	MHRT, MYH7

is a	snp
is	mentioned by
dbSNP	rs730880822
dbSNP (classic)	rs730880822
ClinGen	rs730880822
ebi	rs730880822
HLI	rs730880822
Exac	rs730880822
Gnomad	rs730880822
Varsome	rs730880822
LitVar	rs730880822
Map	rs730880822
PheGenI	rs730880822
Biobank	rs730880822
1000 genomes	rs730880822
hgdp	rs730880822
ensembl	rs730880822
geneview	rs730880822
scholar	rs730880822
google	rs730880822
pharmgkb	rs730880822
gwascentral	rs730880822
openSNP	rs730880822
23andMe	rs730880822
SNPshot	rs730880822
SNPdbe	rs730880822
MSV3d	rs730880822
GWAS Ctlg	rs730880822

Max Magnitude

0

ClinVar
Risk	rs730880822(A;A)
Alt	rs730880822(A;A)
Reference	Rs730880822(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7 MHRT
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23884229C>T
CLNSRC
CLNACC	RCV000158707.2,