rs730880867

Orientation

minus

Stabilized

minus

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

Make rs730880867(A;A)

Make rs730880867(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23429276

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880867
dbSNP (classic)	rs730880867
ClinGen	rs730880867
ebi	rs730880867
HLI	rs730880867
Exac	rs730880867
Gnomad	rs730880867
Varsome	rs730880867
LitVar	rs730880867
Map	rs730880867
PheGenI	rs730880867
Biobank	rs730880867
1000 genomes	rs730880867
hgdp	rs730880867
ensembl	rs730880867
geneview	rs730880867
scholar	rs730880867
google	rs730880867
pharmgkb	rs730880867
gwascentral	rs730880867
openSNP	rs730880867
23andMe	rs730880867
SNPshot	rs730880867
SNPdbe	rs730880867
MSV3d	rs730880867
GWAS Ctlg	rs730880867

Max Magnitude

0

ClinVar
Risk	rs730880867(A;A)
Alt	rs730880867(A;A)
Reference	Rs730880867(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23898485C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000158789.1,