rs730880929

Orientation

minus

Stabilized

minus

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

Make rs730880929(C;C)

Make rs730880929(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23428507

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880929
dbSNP (classic)	rs730880929
ClinGen	rs730880929
ebi	rs730880929
HLI	rs730880929
Exac	rs730880929
Gnomad	rs730880929
Varsome	rs730880929
LitVar	rs730880929
Map	rs730880929
PheGenI	rs730880929
Biobank	rs730880929
1000 genomes	rs730880929
hgdp	rs730880929
ensembl	rs730880929
geneview	rs730880929
scholar	rs730880929
google	rs730880929
pharmgkb	rs730880929
gwascentral	rs730880929
openSNP	rs730880929
23andMe	rs730880929
SNPshot	rs730880929
SNPdbe	rs730880929
MSV3d	rs730880929
GWAS Ctlg	rs730880929

Max Magnitude

0

ClinVar
Risk	rs730880929(C;C)
Alt	rs730880929(C;C)
Reference	Rs730880929(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23897716A>G
CLNSRC
CLNACC	RCV000158889.1,