rs773998062

Orientation

plus

Stabilized

plus

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

Make rs773998062(A;G)

Make rs773998062(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

15760586

Gene

MYH11

is a	snp
is	mentioned by
dbSNP	rs773998062
dbSNP (classic)	rs773998062
ClinGen	rs773998062
ebi	rs773998062
HLI	rs773998062
Exac	rs773998062
Gnomad	rs773998062
Varsome	rs773998062
LitVar	rs773998062
Map	rs773998062
PheGenI	rs773998062
Biobank	rs773998062
1000 genomes	rs773998062
hgdp	rs773998062
ensembl	rs773998062
geneview	rs773998062
scholar	rs773998062
google	rs773998062
pharmgkb	rs773998062
gwascentral	rs773998062
openSNP	rs773998062
23andMe	rs773998062
SNPshot	rs773998062
SNPdbe	rs773998062
MSV3d	rs773998062
GWAS Ctlg	rs773998062

Max Magnitude

0

ClinVar
Risk	rs773998062(G;G) rs773998062(T;T)
Alt	rs773998062(G;G) rs773998062(T;T)
Reference	Rs773998062(A;A)
Significance	Probable-Pathogenic
Disease	not provided not specified
Variation	info
Gene	MYH11
CLNDBN	not provided not specified
Reversed	0
HGVS	NC_000016.9:g.15854443A>G
CLNSRC
CLNACC	RCV000182553.2, RCV000455159.1,