rs730880735

Orientation

minus

Stabilized

minus

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

Make rs730880735(G;G)

Make rs730880735(G;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23425417

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880735
dbSNP (classic)	rs730880735
ClinGen	rs730880735
ebi	rs730880735
HLI	rs730880735
Exac	rs730880735
Gnomad	rs730880735
Varsome	rs730880735
LitVar	rs730880735
Map	rs730880735
PheGenI	rs730880735
Biobank	rs730880735
1000 genomes	rs730880735
hgdp	rs730880735
ensembl	rs730880735
geneview	rs730880735
scholar	rs730880735
google	rs730880735
pharmgkb	rs730880735
gwascentral	rs730880735
openSNP	rs730880735
23andMe	rs730880735
SNPshot	rs730880735
SNPdbe	rs730880735
MSV3d	rs730880735
GWAS Ctlg	rs730880735

Max Magnitude

0

ClinVar
Risk	rs730880735(G;G)
Alt	rs730880735(G;G)
Reference	Rs730880735(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23894626A>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000158525.1,