rs546586969

Orientation

plus

Stabilized

plus

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

Make rs546586969(A;A)

Make rs546586969(A;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23420020

Gene	MIR208B, MYH7

is a	snp
is	mentioned by
dbSNP	rs546586969
dbSNP (classic)	rs546586969
ClinGen	rs546586969
ebi	rs546586969
HLI	rs546586969
Exac	rs546586969
Gnomad	rs546586969
Varsome	rs546586969
LitVar	rs546586969
Map	rs546586969
PheGenI	rs546586969
Biobank	rs546586969
1000 genomes	rs546586969
hgdp	rs546586969
ensembl	rs546586969
geneview	rs546586969
scholar	rs546586969
google	rs546586969
pharmgkb	rs546586969
gwascentral	rs546586969
openSNP	rs546586969
23andMe	rs546586969
SNPshot	rs546586969
SNPdbe	rs546586969
MSV3d	rs546586969
GWAS Ctlg	rs546586969

Max Magnitude

0

ClinVar
Risk	rs546586969(A;A)
Alt	rs546586969(A;A)
Reference	Rs546586969(T;T)
Significance	Probable-Pathogenic
Disease	not provided not specified
Variation	info
Gene	MYH7 MIR208B
CLNDBN	not provided not specified
Reversed	0
HGVS	NC_000014.8:g.23889229T>A
CLNSRC
CLNACC	RCV000158610.1, RCV000223885.1,