rs758888662

Orientation

plus

Stabilized

plus

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

Make rs758888662(C;T)

Make rs758888662(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

10523495

Gene	MYHAS, MYH2

is a	snp
is	mentioned by
dbSNP	rs758888662
dbSNP (classic)	rs758888662
ClinGen	rs758888662
ebi	rs758888662
HLI	rs758888662
Exac	rs758888662
Gnomad	rs758888662
Varsome	rs758888662
LitVar	rs758888662
Map	rs758888662
PheGenI	rs758888662
Biobank	rs758888662
1000 genomes	rs758888662
hgdp	rs758888662
ensembl	rs758888662
geneview	rs758888662
scholar	rs758888662
google	rs758888662
pharmgkb	rs758888662
gwascentral	rs758888662
openSNP	rs758888662
23andMe	rs758888662
SNPshot	rs758888662
SNPdbe	rs758888662
MSV3d	rs758888662
GWAS Ctlg	rs758888662

Max Magnitude

0

ClinVar
Risk	rs758888662(T;T)
Alt	rs758888662(T;T)
Reference	Rs758888662(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH2 MYHAS
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.10426812C>T
CLNSRC
CLNACC	RCV000487929.1,