rs201082272

Orientation

plus

Stabilized

plus

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

Make rs201082272(C;G)

Make rs201082272(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

10535366

Gene	MYHAS, MYH2

is a	snp
is	mentioned by
dbSNP	rs201082272
dbSNP (classic)	rs201082272
ClinGen	rs201082272
ebi	rs201082272
HLI	rs201082272
Exac	rs201082272
Gnomad	rs201082272
Varsome	rs201082272
LitVar	rs201082272
Map	rs201082272
PheGenI	rs201082272
Biobank	rs201082272
1000 genomes	rs201082272
hgdp	rs201082272
ensembl	rs201082272
geneview	rs201082272
scholar	rs201082272
google	rs201082272
pharmgkb	rs201082272
gwascentral	rs201082272
openSNP	rs201082272
23andMe	rs201082272
SNPshot	rs201082272
SNPdbe	rs201082272
MSV3d	rs201082272
GWAS Ctlg	rs201082272

Max Magnitude

0

ClinVar
Risk	rs201082272(G;G) rs201082272(T;T)
Alt	rs201082272(G;G) rs201082272(T;T)
Reference	Rs201082272(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH2 MYHAS
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.10438683C>G
CLNSRC
CLNACC	RCV000413648.1,