rs387906532

Orientation

minus

Stabilized

minus

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

Make rs387906532(C;C)

Make rs387906532(C;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

15726936

Gene

MYH11

is a	snp
is	mentioned by
dbSNP	rs387906532
dbSNP (classic)	rs387906532
ClinGen	rs387906532
ebi	rs387906532
HLI	rs387906532
Exac	rs387906532
Gnomad	rs387906532
Varsome	rs387906532
LitVar	rs387906532
Map	rs387906532
PheGenI	rs387906532
Biobank	rs387906532
1000 genomes	rs387906532
hgdp	rs387906532
ensembl	rs387906532
geneview	rs387906532
scholar	rs387906532
google	rs387906532
pharmgkb	rs387906532
gwascentral	rs387906532
openSNP	rs387906532
23andMe	rs387906532
SNPshot	rs387906532
SNPdbe	rs387906532
MSV3d	rs387906532
GWAS Ctlg	rs387906532

Max Magnitude

0

ClinVar
Risk	rs387906532(C;C)
Alt	rs387906532(C;C)
Reference	Rs387906532(T;T)
Significance	Pathogenic
Disease	Aortic aneurysm
Variation	info
Gene	MYH11
CLNDBN	Aortic aneurysm, familial thoracic 4
Reversed	1
HGVS	NC_000016.9:g.15820793A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015194.25,