rs730880869

Orientation

minus

Stabilized

minus

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

Make rs730880869(A;T)

Make rs730880869(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23429252

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880869
dbSNP (classic)	rs730880869
ClinGen	rs730880869
ebi	rs730880869
HLI	rs730880869
Exac	rs730880869
Gnomad	rs730880869
Varsome	rs730880869
LitVar	rs730880869
Map	rs730880869
PheGenI	rs730880869
Biobank	rs730880869
1000 genomes	rs730880869
hgdp	rs730880869
ensembl	rs730880869
geneview	rs730880869
scholar	rs730880869
google	rs730880869
pharmgkb	rs730880869
gwascentral	rs730880869
openSNP	rs730880869
23andMe	rs730880869
SNPshot	rs730880869
SNPdbe	rs730880869
MSV3d	rs730880869
GWAS Ctlg	rs730880869

Max Magnitude

0

ClinVar
Risk	rs730880869(T;T)
Alt	rs730880869(T;T)
Reference	Rs730880869(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23898461T>A; NC_000014.8:g.23898461T>C
CLNSRC
CLNACC	RCV000158791.2, RCV000493381.1,