rs727504261

Orientation

minus

Stabilized

minus

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

Make rs727504261(A;G)

Make rs727504261(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23424121

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs727504261
dbSNP (classic)	rs727504261
ClinGen	rs727504261
ebi	rs727504261
HLI	rs727504261
Exac	rs727504261
Gnomad	rs727504261
Varsome	rs727504261
LitVar	rs727504261
Map	rs727504261
PheGenI	rs727504261
Biobank	rs727504261
1000 genomes	rs727504261
hgdp	rs727504261
ensembl	rs727504261
geneview	rs727504261
scholar	rs727504261
google	rs727504261
pharmgkb	rs727504261
gwascentral	rs727504261
openSNP	rs727504261
23andMe	rs727504261
SNPshot	rs727504261
SNPdbe	rs727504261
MSV3d	rs727504261
GWAS Ctlg	rs727504261

Max Magnitude

0

ClinVar
Risk	rs727504261(G;G)
Alt	rs727504261(G;G)
Reference	Rs727504261(A;A)
Significance	Pathogenic
Disease	not specified
Variation	info
Gene	MYH7
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23893330T>C
CLNSRC
CLNACC	RCV000154244.2,