rs267606902

Orientation

minus

Stabilized

minus

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

Make rs267606902(A;A)

Make rs267606902(A;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

15748092

Gene

MYH11

is a	snp
is	mentioned by
dbSNP	rs267606902
dbSNP (classic)	rs267606902
ClinGen	rs267606902
ebi	rs267606902
HLI	rs267606902
Exac	rs267606902
Gnomad	rs267606902
Varsome	rs267606902
LitVar	rs267606902
Map	rs267606902
PheGenI	rs267606902
Biobank	rs267606902
1000 genomes	rs267606902
hgdp	rs267606902
ensembl	rs267606902
geneview	rs267606902
scholar	rs267606902
google	rs267606902
pharmgkb	rs267606902
gwascentral	rs267606902
openSNP	rs267606902
23andMe	rs267606902
SNPshot	rs267606902
SNPdbe	rs267606902
MSV3d	rs267606902
GWAS Ctlg	rs267606902

Max Magnitude

0

ClinVar
Risk	rs267606902(A;A)
Alt	rs267606902(A;A)
Reference	Rs267606902(G;G)
Significance	Other
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.15841949C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015196.25, RCV000157330.2,