rs730880920

Orientation

minus

Stabilized

minus

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

Make rs730880920(A;A)

Make rs730880920(A;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23432647

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880920
dbSNP (classic)	rs730880920
ClinGen	rs730880920
ebi	rs730880920
HLI	rs730880920
Exac	rs730880920
Gnomad	rs730880920
Varsome	rs730880920
LitVar	rs730880920
Map	rs730880920
PheGenI	rs730880920
Biobank	rs730880920
1000 genomes	rs730880920
hgdp	rs730880920
ensembl	rs730880920
geneview	rs730880920
scholar	rs730880920
google	rs730880920
pharmgkb	rs730880920
gwascentral	rs730880920
openSNP	rs730880920
23andMe	rs730880920
SNPshot	rs730880920
SNPdbe	rs730880920
MSV3d	rs730880920
GWAS Ctlg	rs730880920

Max Magnitude

0

ClinVar
Risk	rs730880920(A;A)
Alt	rs730880920(A;A)
Reference	Rs730880920(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23901856A>T
CLNSRC
CLNACC	RCV000158877.1,