rs730880898

Orientation

minus

Stabilized

minus

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

Make rs730880898(A;A)

Make rs730880898(A;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23424970

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880898
dbSNP (classic)	rs730880898
ClinGen	rs730880898
ebi	rs730880898
HLI	rs730880898
Exac	rs730880898
Gnomad	rs730880898
Varsome	rs730880898
LitVar	rs730880898
Map	rs730880898
PheGenI	rs730880898
Biobank	rs730880898
1000 genomes	rs730880898
hgdp	rs730880898
ensembl	rs730880898
geneview	rs730880898
scholar	rs730880898
google	rs730880898
pharmgkb	rs730880898
gwascentral	rs730880898
openSNP	rs730880898
23andMe	rs730880898
SNPshot	rs730880898
SNPdbe	rs730880898
MSV3d	rs730880898
GWAS Ctlg	rs730880898

Max Magnitude

0

ClinVar
Risk	rs730880898(A;A)
Alt	rs730880898(A;A)
Reference	Rs730880898(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23894179A>T
CLNSRC
CLNACC	RCV000158844.1,