rs267606901

Orientation

minus

Stabilized

minus

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

Make rs267606901(G;T)

Make rs267606901(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

15726882

Gene

MYH11

is a	snp
is	mentioned by
dbSNP	rs267606901
dbSNP (classic)	rs267606901
ClinGen	rs267606901
ebi	rs267606901
HLI	rs267606901
Exac	rs267606901
Gnomad	rs267606901
Varsome	rs267606901
LitVar	rs267606901
Map	rs267606901
PheGenI	rs267606901
Biobank	rs267606901
1000 genomes	rs267606901
hgdp	rs267606901
ensembl	rs267606901
geneview	rs267606901
scholar	rs267606901
google	rs267606901
pharmgkb	rs267606901
gwascentral	rs267606901
openSNP	rs267606901
23andMe	rs267606901
SNPshot	rs267606901
SNPdbe	rs267606901
MSV3d	rs267606901
GWAS Ctlg	rs267606901

Max Magnitude

0

ClinVar
Risk	rs267606901(T;T)
Alt	rs267606901(T;T)
Reference	Rs267606901(G;G)
Significance	Pathogenic
Disease	Aortic aneurysm Thoracic aortic aneurysm and aortic dissection
Variation	info
Gene	MYH11
CLNDBN	Aortic aneurysm, familial thoracic 4 Thoracic aortic aneurysm and aortic dissection
Reversed	1
HGVS	NC_000016.9:g.15820739C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015195.25, RCV000251625.1,