rs370069461

Orientation

plus

Stabilized

plus

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

Make rs370069461(C;T)

Make rs370069461(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

14

Position

23417669

Gene	MHRT, MIR208B, MYH7

is a	snp
is	mentioned by
dbSNP	rs370069461
dbSNP (classic)	rs370069461
ClinGen	rs370069461
ebi	rs370069461
HLI	rs370069461
Exac	rs370069461
Gnomad	rs370069461
Varsome	rs370069461
LitVar	rs370069461
Map	rs370069461
PheGenI	rs370069461
Biobank	rs370069461
1000 genomes	rs370069461
hgdp	rs370069461
ensembl	rs370069461
geneview	rs370069461
scholar	rs370069461
google	rs370069461
pharmgkb	rs370069461
gwascentral	rs370069461
openSNP	rs370069461
23andMe	rs370069461
SNPshot	rs370069461
SNPdbe	rs370069461
MSV3d	rs370069461
GWAS Ctlg	rs370069461

Max Magnitude

0

ClinVar
Risk	rs370069461(T;T)
Alt	rs370069461(T;T)
Reference	Rs370069461(C;C)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	MYH7 MHRT MIR208B
CLNDBN	not specified
Reversed	0
HGVS	NC_000014.8:g.23886878C>T
CLNSRC
CLNACC	RCV000158641.3,