rs121434456

Orientation

plus

Stabilized

plus

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

Make rs121434456(A;G)

Make rs121434456(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

10438

is a	snp
is	mentioned by
dbSNP	rs121434456
dbSNP (classic)	rs121434456
ClinGen	rs121434456
ebi	rs121434456
HLI	rs121434456
Exac	rs121434456
Gnomad	rs121434456
Varsome	rs121434456
LitVar	rs121434456
Map	rs121434456
PheGenI	rs121434456
Biobank	rs121434456
1000 genomes	rs121434456
hgdp	rs121434456
ensembl	rs121434456
geneview	rs121434456
scholar	rs121434456
google	rs121434456
pharmgkb	rs121434456
gwascentral	rs121434456
openSNP	rs121434456
23andMe	rs121434456
SNPshot	rs121434456
SNPdbe	rs121434456
MSV3d	rs121434456
GWAS Ctlg	rs121434456

Max Magnitude

0

ClinVar
Risk	rs121434456(G;G)
Alt	rs121434456(G;G)
Reference	Rs121434456(A;A)
Significance	Pathogenic
Disease	Mitochondrial encephalomyopathy
Variation	info
Gene
CLNDBN	Mitochondrial encephalomyopathy
Reversed	0
HGVS	NC_012920.1:m.10438A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010249.2,