rs121434476

Orientation

plus

Stabilized

plus

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

Make rs121434476(C;C)

Make rs121434476(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

10010

is a	snp
is	mentioned by
dbSNP	rs121434476
dbSNP (classic)	rs121434476
ClinGen	rs121434476
ebi	rs121434476
HLI	rs121434476
Exac	rs121434476
Gnomad	rs121434476
Varsome	rs121434476
LitVar	rs121434476
Map	rs121434476
PheGenI	rs121434476
Biobank	rs121434476
1000 genomes	rs121434476
hgdp	rs121434476
ensembl	rs121434476
geneview	rs121434476
scholar	rs121434476
google	rs121434476
pharmgkb	rs121434476
gwascentral	rs121434476
openSNP	rs121434476
23andMe	rs121434476
SNPshot	rs121434476
SNPdbe	rs121434476
MSV3d	rs121434476
GWAS Ctlg	rs121434476

Max Magnitude

0

ClinVar
Risk	rs121434476(C;C)
Alt	rs121434476(C;C)
Reference	Rs121434476(T;T)
Significance	Pathogenic
Disease	Exercise intolerance
Variation	info
Gene
CLNDBN	Exercise intolerance
Reversed	0
HGVS	NC_012920.1:m.10010T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010236.4,