rs397516178

Orientation

minus

Stabilized

minus

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

Make rs397516178(G;T)

Make rs397516178(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23422291

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs397516178
dbSNP (classic)	rs397516178
ClinGen	rs397516178
ebi	rs397516178
HLI	rs397516178
Exac	rs397516178
Gnomad	rs397516178
Varsome	rs397516178
LitVar	rs397516178
Map	rs397516178
PheGenI	rs397516178
Biobank	rs397516178
1000 genomes	rs397516178
hgdp	rs397516178
ensembl	rs397516178
geneview	rs397516178
scholar	rs397516178
google	rs397516178
pharmgkb	rs397516178
gwascentral	rs397516178
openSNP	rs397516178
23andMe	rs397516178
SNPshot	rs397516178
SNPdbe	rs397516178
MSV3d	rs397516178
GWAS Ctlg	rs397516178

Max Magnitude

0

ClinVar
Risk	rs397516178(A;A) rs397516178(T;T)
Alt	rs397516178(A;A) rs397516178(T;T)
Reference	Rs397516178(G;G)
Significance	Pathogenic
Disease	not specified
Variation	info
Gene	MYH7
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23891500C>A
CLNSRC	ClinVar
CLNACC	RCV000035841.3,