rs121434471

Orientation

plus

Stabilized

plus

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

Make rs121434471(C;C)

Make rs121434471(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

4291

is a	snp
is	mentioned by
dbSNP	rs121434471
dbSNP (classic)	rs121434471
ClinGen	rs121434471
ebi	rs121434471
HLI	rs121434471
Exac	rs121434471
Gnomad	rs121434471
Varsome	rs121434471
LitVar	rs121434471
Map	rs121434471
PheGenI	rs121434471
Biobank	rs121434471
1000 genomes	rs121434471
hgdp	rs121434471
ensembl	rs121434471
geneview	rs121434471
scholar	rs121434471
google	rs121434471
pharmgkb	rs121434471
gwascentral	rs121434471
openSNP	rs121434471
23andMe	rs121434471
SNPshot	rs121434471
SNPdbe	rs121434471
MSV3d	rs121434471
GWAS Ctlg	rs121434471

Max Magnitude

0

ClinVar
Risk	rs121434471(C;C)
Alt	rs121434471(C;C)
Reference	Rs121434471(T;T)
Significance	Pathogenic
Disease	Hypertension
Variation	info
Gene
CLNDBN	Hypertension, hypercholesterolemia, and hypomagnesemia, mitochondrial
Reversed	0
HGVS	NC_012920.1:m.4291T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010230.2,