rs145677314

Orientation

plus

Stabilized

plus

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

Make rs145677314(A;A)

Make rs145677314(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23425346

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs145677314
dbSNP (classic)	rs145677314
ClinGen	rs145677314
ebi	rs145677314
HLI	rs145677314
Exac	rs145677314
Gnomad	rs145677314
Varsome	rs145677314
LitVar	rs145677314
Map	rs145677314
PheGenI	rs145677314
Biobank	rs145677314
1000 genomes	rs145677314
hgdp	rs145677314
ensembl	rs145677314
geneview	rs145677314
scholar	rs145677314
google	rs145677314
pharmgkb	rs145677314
gwascentral	rs145677314
openSNP	rs145677314
23andMe	rs145677314
SNPshot	rs145677314
SNPdbe	rs145677314
MSV3d	rs145677314
GWAS Ctlg	rs145677314

Max Magnitude

0

ClinVar
Risk	rs145677314(A;A)
Alt	rs145677314(A;A)
Reference	Rs145677314(G;G)
Significance	Other
Disease	Primary familial hypertrophic cardiomyopathy not specified Hypertrophic cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	Primary familial hypertrophic cardiomyopathy not specified Hypertrophic cardiomyopathy
Reversed	0
HGVS	NC_000014.8:g.23894555G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000148709.2, RCV000154774.4, RCV000231165.1,