rs730880849

Orientation

minus

Stabilized

minus

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

Make rs730880849(C;C)

Make rs730880849(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23431587

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880849
dbSNP (classic)	rs730880849
ClinGen	rs730880849
ebi	rs730880849
HLI	rs730880849
Exac	rs730880849
Gnomad	rs730880849
Varsome	rs730880849
LitVar	rs730880849
Map	rs730880849
PheGenI	rs730880849
Biobank	rs730880849
1000 genomes	rs730880849
hgdp	rs730880849
ensembl	rs730880849
geneview	rs730880849
scholar	rs730880849
google	rs730880849
pharmgkb	rs730880849
gwascentral	rs730880849
openSNP	rs730880849
23andMe	rs730880849
SNPshot	rs730880849
SNPdbe	rs730880849
MSV3d	rs730880849
GWAS Ctlg	rs730880849

Max Magnitude

0

ClinVar
Risk	rs730880849(C;C)
Alt	rs730880849(C;C)
Reference	Rs730880849(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23900796A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000158757.2,