rs397516141

Orientation

minus

Stabilized

minus

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

Make rs397516141(A;C)

Make rs397516141(C;C)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23425409

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs397516141
dbSNP (classic)	rs397516141
ClinGen	rs397516141
ebi	rs397516141
HLI	rs397516141
Exac	rs397516141
Gnomad	rs397516141
Varsome	rs397516141
LitVar	rs397516141
Map	rs397516141
PheGenI	rs397516141
Biobank	rs397516141
1000 genomes	rs397516141
hgdp	rs397516141
ensembl	rs397516141
geneview	rs397516141
scholar	rs397516141
google	rs397516141
pharmgkb	rs397516141
gwascentral	rs397516141
openSNP	rs397516141
23andMe	rs397516141
SNPshot	rs397516141
SNPdbe	rs397516141
MSV3d	rs397516141
GWAS Ctlg	rs397516141

Max Magnitude

0

ClinVar
Risk	rs397516141(C;C)
Alt	rs397516141(C;C)
Reference	Rs397516141(A;A)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	MYH7
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23894618T>G
CLNSRC	ClinVar
CLNACC	RCV000035782.4,