rs1057519221

Orientation

minus

Stabilized

minus

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

Make rs1057519221(A;A)

Make rs1057519221(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

23432796

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs1057519221
dbSNP (classic)	rs1057519221
ClinGen	rs1057519221
ebi	rs1057519221
HLI	rs1057519221
Exac	rs1057519221
Gnomad	rs1057519221
Varsome	rs1057519221
LitVar	rs1057519221
Map	rs1057519221
PheGenI	rs1057519221
Biobank	rs1057519221
1000 genomes	rs1057519221
hgdp	rs1057519221
ensembl	rs1057519221
geneview	rs1057519221
scholar	rs1057519221
google	rs1057519221
pharmgkb	rs1057519221
gwascentral	rs1057519221
openSNP	rs1057519221
23andMe	rs1057519221
SNPshot	rs1057519221
SNPdbe	rs1057519221
MSV3d	rs1057519221
GWAS Ctlg	rs1057519221

Max Magnitude

0

ClinVar
Risk	rs1057519221(A;A)
Alt	rs1057519221(A;A)
Reference	Rs1057519221(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23902005C>T
CLNSRC
CLNACC	RCV000415886.1,