rs730880774

Orientation

minus

Stabilized

minus

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

Make rs730880774(A;A)

Make rs730880774(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23420147

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880774
dbSNP (classic)	rs730880774
ClinGen	rs730880774
ebi	rs730880774
HLI	rs730880774
Exac	rs730880774
Gnomad	rs730880774
Varsome	rs730880774
LitVar	rs730880774
Map	rs730880774
PheGenI	rs730880774
Biobank	rs730880774
1000 genomes	rs730880774
hgdp	rs730880774
ensembl	rs730880774
geneview	rs730880774
scholar	rs730880774
google	rs730880774
pharmgkb	rs730880774
gwascentral	rs730880774
openSNP	rs730880774
23andMe	rs730880774
SNPshot	rs730880774
SNPdbe	rs730880774
MSV3d	rs730880774
GWAS Ctlg	rs730880774

Max Magnitude

0

ClinVar
Risk	rs730880774(A;A)
Alt	rs730880774(A;A)
Reference	Rs730880774(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23889356C>T
CLNSRC
CLNACC	RCV000158606.2,