rs121434466

Orientation

plus

Stabilized

plus

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

Make rs121434466(A;G)

Make rs121434466(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

4269

is a	snp
is	mentioned by
dbSNP	rs121434466
dbSNP (classic)	rs121434466
ClinGen	rs121434466
ebi	rs121434466
HLI	rs121434466
Exac	rs121434466
Gnomad	rs121434466
Varsome	rs121434466
LitVar	rs121434466
Map	rs121434466
PheGenI	rs121434466
Biobank	rs121434466
1000 genomes	rs121434466
hgdp	rs121434466
ensembl	rs121434466
geneview	rs121434466
scholar	rs121434466
google	rs121434466
pharmgkb	rs121434466
gwascentral	rs121434466
openSNP	rs121434466
23andMe	rs121434466
SNPshot	rs121434466
SNPdbe	rs121434466
MSV3d	rs121434466
GWAS Ctlg	rs121434466

Max Magnitude

0

ClinVar
Risk	rs121434466(G;G)
Alt	rs121434466(G;G)
Reference	Rs121434466(A;A)
Significance	Pathogenic
Disease	Cardiomyopathy
Variation	info
Gene
CLNDBN	Cardiomyopathy, fatal
Reversed	0
HGVS	NC_012920.1:m.4269A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010225.4,