rs193922629

Orientation

minus

Stabilized

minus

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

Make rs193922629(C;C)

Make rs193922629(C;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

15737509

Gene

MYH11

is a	snp
is	mentioned by
dbSNP	rs193922629
dbSNP (classic)	rs193922629
ClinGen	rs193922629
ebi	rs193922629
HLI	rs193922629
Exac	rs193922629
Gnomad	rs193922629
Varsome	rs193922629
LitVar	rs193922629
Map	rs193922629
PheGenI	rs193922629
Biobank	rs193922629
1000 genomes	rs193922629
hgdp	rs193922629
ensembl	rs193922629
geneview	rs193922629
scholar	rs193922629
google	rs193922629
pharmgkb	rs193922629
gwascentral	rs193922629
openSNP	rs193922629
23andMe	rs193922629
SNPshot	rs193922629
SNPdbe	rs193922629
MSV3d	rs193922629
GWAS Ctlg	rs193922629

Max Magnitude

0

ClinVar
Risk	rs193922629(C;C)
Alt	rs193922629(C;C)
Reference	Rs193922629(T;T)
Significance	Probable-Pathogenic
Disease	Familial aortopathy
Variation	info
Gene	MYH11
CLNDBN	Familial aortopathy
Reversed	1
HGVS	NC_000016.9:g.15831366A>G
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030296.1,