rs727503277

Orientation

minus

Stabilized

minus

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

Make rs727503277(C;T)

Make rs727503277(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23431768

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs727503277
dbSNP (classic)	rs727503277
ClinGen	rs727503277
ebi	rs727503277
HLI	rs727503277
Exac	rs727503277
Gnomad	rs727503277
Varsome	rs727503277
LitVar	rs727503277
Map	rs727503277
PheGenI	rs727503277
Biobank	rs727503277
1000 genomes	rs727503277
hgdp	rs727503277
ensembl	rs727503277
geneview	rs727503277
scholar	rs727503277
google	rs727503277
pharmgkb	rs727503277
gwascentral	rs727503277
openSNP	rs727503277
23andMe	rs727503277
SNPshot	rs727503277
SNPdbe	rs727503277
MSV3d	rs727503277
GWAS Ctlg	rs727503277

Max Magnitude

0

ClinVar
Risk	rs727503277(T;T)
Alt	rs727503277(T;T)
Reference	Rs727503277(C;C)
Significance	Pathogenic
Disease	not specified
Variation	info
Gene	MYH7
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23900977G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000151310.3,