rs397516268

Orientation

minus

Stabilized

minus

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

Make rs397516268(A;G)

Make rs397516268(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23431466

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs397516268
dbSNP (classic)	rs397516268
ClinGen	rs397516268
ebi	rs397516268
HLI	rs397516268
Exac	rs397516268
Gnomad	rs397516268
Varsome	rs397516268
LitVar	rs397516268
Map	rs397516268
PheGenI	rs397516268
Biobank	rs397516268
1000 genomes	rs397516268
hgdp	rs397516268
ensembl	rs397516268
geneview	rs397516268
scholar	rs397516268
google	rs397516268
pharmgkb	rs397516268
gwascentral	rs397516268
openSNP	rs397516268
23andMe	rs397516268
SNPshot	rs397516268
SNPdbe	rs397516268
MSV3d	rs397516268
GWAS Ctlg	rs397516268

Max Magnitude

0

ClinVar
Risk	rs397516268(G;G) rs397516268(T;T)
Alt	rs397516268(G;G) rs397516268(T;T)
Reference	Rs397516268(A;A)
Significance	Probable-Pathogenic
Disease	not provided not specified
Variation	info
Gene	MYH7
CLNDBN	not provided not specified
Reversed	1
HGVS	NC_000014.8:g.23900675T>A; NC_000014.8:g.23900675T>C
CLNSRC
CLNACC	RCV000158762.1, RCV000036001.3,