rs786205435

Orientation

minus

Stabilized

minus

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

Make rs786205435(A;T)

Make rs786205435(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

15732617

Gene

MYH11

is a	snp
is	mentioned by
dbSNP	rs786205435
dbSNP (classic)	rs786205435
ClinGen	rs786205435
ebi	rs786205435
HLI	rs786205435
Exac	rs786205435
Gnomad	rs786205435
Varsome	rs786205435
LitVar	rs786205435
Map	rs786205435
PheGenI	rs786205435
Biobank	rs786205435
1000 genomes	rs786205435
hgdp	rs786205435
ensembl	rs786205435
geneview	rs786205435
scholar	rs786205435
google	rs786205435
pharmgkb	rs786205435
gwascentral	rs786205435
openSNP	rs786205435
23andMe	rs786205435
SNPshot	rs786205435
SNPdbe	rs786205435
MSV3d	rs786205435
GWAS Ctlg	rs786205435

Max Magnitude

0

ClinVar
Risk	rs786205435(T;T)
Alt	rs786205435(T;T)
Reference	Rs786205435(A;A)
Significance	Probable-Pathogenic
Disease	Visceral myopathy
Variation	info
Gene	MYH11
CLNDBN	Visceral myopathy
Reversed	1
HGVS	NC_000016.9:g.15826474T>A
CLNSRC	Hospital Sainte-Justine
CLNACC	RCV000172830.1,