rs730880916

Orientation

minus

Stabilized

minus

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

Make rs730880916(A;A)

Make rs730880916(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23415410

Gene	MHRT, MYH7

is a	snp
is	mentioned by
dbSNP	rs730880916
dbSNP (classic)	rs730880916
ClinGen	rs730880916
ebi	rs730880916
HLI	rs730880916
Exac	rs730880916
Gnomad	rs730880916
Varsome	rs730880916
LitVar	rs730880916
Map	rs730880916
PheGenI	rs730880916
Biobank	rs730880916
1000 genomes	rs730880916
hgdp	rs730880916
ensembl	rs730880916
geneview	rs730880916
scholar	rs730880916
google	rs730880916
pharmgkb	rs730880916
gwascentral	rs730880916
openSNP	rs730880916
23andMe	rs730880916
SNPshot	rs730880916
SNPdbe	rs730880916
MSV3d	rs730880916
GWAS Ctlg	rs730880916

Max Magnitude

0

ClinVar
Risk	rs730880916(A;A)
Alt	rs730880916(A;A)
Reference	Rs730880916(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7 MHRT
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23884619C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000158871.2,