rs727504425

Orientation

minus

Stabilized

minus

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

Make rs727504425(G;T)

Make rs727504425(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

110915721

Gene

MYL2

is a	snp
is	mentioned by
dbSNP	rs727504425
dbSNP (classic)	rs727504425
ClinGen	rs727504425
ebi	rs727504425
HLI	rs727504425
Exac	rs727504425
Gnomad	rs727504425
Varsome	rs727504425
LitVar	rs727504425
Map	rs727504425
PheGenI	rs727504425
Biobank	rs727504425
1000 genomes	rs727504425
hgdp	rs727504425
ensembl	rs727504425
geneview	rs727504425
scholar	rs727504425
google	rs727504425
pharmgkb	rs727504425
gwascentral	rs727504425
openSNP	rs727504425
23andMe	rs727504425
SNPshot	rs727504425
SNPdbe	rs727504425
MSV3d	rs727504425
GWAS Ctlg	rs727504425

Max Magnitude

0

ClinVar
Risk	rs727504425(T;T)
Alt	rs727504425(T;T)
Reference	Rs727504425(G;G)
Significance	Probable-Pathogenic
Disease	not specified not provided
Variation	info
Gene	MYL2
CLNDBN	not specified not provided
Reversed	1
HGVS	NC_000012.11:g.111353525C>A
CLNSRC
CLNACC	RCV000154622.2, RCV000489222.1,