rs587776436

Merged into

rs370471013

Orientation

minus

Stabilized

plus

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

Make rs587776436(C;C)

Make rs587776436(C;T)

Make rs587776436(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

5559

is a	snp
is	mentioned by
dbSNP	rs587776436
dbSNP (classic)	rs587776436
ClinGen	rs587776436
ebi	rs587776436
HLI	rs587776436
Exac	rs587776436
Gnomad	rs587776436
Varsome	rs587776436
LitVar	rs587776436
Map	rs587776436
PheGenI	rs587776436
Biobank	rs587776436
1000 genomes	rs587776436
hgdp	rs587776436
ensembl	rs587776436
geneview	rs587776436
scholar	rs587776436
google	rs587776436
pharmgkb	rs587776436
gwascentral	rs587776436
openSNP	rs587776436
23andMe	rs587776436
SNPshot	rs587776436
SNPdbe	rs587776436
MSV3d	rs587776436
GWAS Ctlg	rs587776436

Status

Merged into rs370471013

Max Magnitude

0

ClinVar
Risk	rs587776436(G;G)
Alt	rs587776436(G;G)
Reference	Rs587776436(A;A)
Significance	Pathogenic
Disease	Leigh's disease
Variation	info
Gene
CLNDBN	Leigh's disease
Reversed	0
HGVS	NC_012920.1:m.5559A>G
CLNSRC
CLNACC	RCV000144003.2,