rs397516408

Orientation

minus

Stabilized

minus

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

Make rs397516408(A;G)

Make rs397516408(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

110919117

Gene

MYL2

is a	snp
is	mentioned by
dbSNP	rs397516408
dbSNP (classic)	rs397516408
ClinGen	rs397516408
ebi	rs397516408
HLI	rs397516408
Exac	rs397516408
Gnomad	rs397516408
Varsome	rs397516408
LitVar	rs397516408
Map	rs397516408
PheGenI	rs397516408
Biobank	rs397516408
1000 genomes	rs397516408
hgdp	rs397516408
ensembl	rs397516408
geneview	rs397516408
scholar	rs397516408
google	rs397516408
pharmgkb	rs397516408
gwascentral	rs397516408
openSNP	rs397516408
23andMe	rs397516408
SNPshot	rs397516408
SNPdbe	rs397516408
MSV3d	rs397516408
GWAS Ctlg	rs397516408

Max Magnitude

0

ClinVar
Risk	rs397516408(G;G)
Alt	rs397516408(G;G)
Reference	Rs397516408(A;A)
Significance	Probable-Pathogenic
Disease	Primary familial hypertrophic cardiomyopathy
Variation	info
Gene	MYL2
CLNDBN	Primary familial hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000012.11:g.111356921T>C
CLNSRC	ClinVar
CLNACC	RCV000036410.2,