rs199476416

Orientation

plus

Stabilized

plus

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

Make rs199476416(C;C)

Make rs199476416(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

68206903

Gene

MYPN

is a	snp
is	mentioned by
dbSNP	rs199476416
dbSNP (classic)	rs199476416
ClinGen	rs199476416
ebi	rs199476416
HLI	rs199476416
Exac	rs199476416
Gnomad	rs199476416
Varsome	rs199476416
LitVar	rs199476416
Map	rs199476416
PheGenI	rs199476416
Biobank	rs199476416
1000 genomes	rs199476416
hgdp	rs199476416
ensembl	rs199476416
geneview	rs199476416
scholar	rs199476416
google	rs199476416
pharmgkb	rs199476416
gwascentral	rs199476416
openSNP	rs199476416
23andMe	rs199476416
SNPshot	rs199476416
SNPdbe	rs199476416
MSV3d	rs199476416
GWAS Ctlg	rs199476416

Max Magnitude

0

ClinVar
Risk	rs199476416(A;A) rs199476416(C;C)
Alt	rs199476416(A;A) rs199476416(C;C)
Reference	Rs199476416(G;G)
Significance	Probable-Pathogenic
Disease	not provided Dilated cardiomyopathy 1KK
Variation	info
Gene	MYPN
CLNDBN	not provided Dilated cardiomyopathy 1KK
Reversed	0
HGVS	NC_000010.10:g.69966660G>A; NC_000010.10:g.69966660G>C
CLNSRC	Leiden Muscular Dystrophy pages (MYPN)
CLNACC	RCV000183599.2, RCV000024507.1, RCV000207010.1,