rs786205484

Orientation

minus

Stabilized

minus

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

Make rs786205484(A;A)

Make rs786205484(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

23400916

Gene

MYH6

is a	snp
is	mentioned by
dbSNP	rs786205484
dbSNP (classic)	rs786205484
ClinGen	rs786205484
ebi	rs786205484
HLI	rs786205484
Exac	rs786205484
Gnomad	rs786205484
Varsome	rs786205484
LitVar	rs786205484
Map	rs786205484
PheGenI	rs786205484
Biobank	rs786205484
1000 genomes	rs786205484
hgdp	rs786205484
ensembl	rs786205484
geneview	rs786205484
scholar	rs786205484
google	rs786205484
pharmgkb	rs786205484
gwascentral	rs786205484
openSNP	rs786205484
23andMe	rs786205484
SNPshot	rs786205484
SNPdbe	rs786205484
MSV3d	rs786205484
GWAS Ctlg	rs786205484

Max Magnitude

0

ClinVar
Risk	rs786205484(A;A)
Alt	rs786205484(A;A)
Reference	Rs786205484(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH6
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23870125G>T
CLNSRC
CLNACC	RCV000171219.1,