rs121434462

Orientation

plus

Stabilized

plus

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

Make rs121434462(A;A)

Make rs121434462(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

12315

is a	snp
is	mentioned by
dbSNP	rs121434462
dbSNP (classic)	rs121434462
ClinGen	rs121434462
ebi	rs121434462
HLI	rs121434462
Exac	rs121434462
Gnomad	rs121434462
Varsome	rs121434462
LitVar	rs121434462
Map	rs121434462
PheGenI	rs121434462
Biobank	rs121434462
1000 genomes	rs121434462
hgdp	rs121434462
ensembl	rs121434462
geneview	rs121434462
scholar	rs121434462
google	rs121434462
pharmgkb	rs121434462
gwascentral	rs121434462
openSNP	rs121434462
23andMe	rs121434462
SNPshot	rs121434462
SNPdbe	rs121434462
MSV3d	rs121434462
GWAS Ctlg	rs121434462

Max Magnitude

0

ClinVar
Risk	rs121434462(A;A)
Alt	rs121434462(A;A)
Reference	Rs121434462(G;G)
Significance	Pathogenic
Disease	Mitochondrial encephalomyopathy
Variation	info
Gene
CLNDBN	Mitochondrial encephalomyopathy
Reversed	0
HGVS	NC_012920.1:m.12315G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010203.4,