rs863225446

Orientation

minus

Stabilized

minus

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

Make rs863225446(A;G)

Make rs863225446(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

43960534

Gene

LRPPRC

is a	snp
is	mentioned by
dbSNP	rs863225446
dbSNP (classic)	rs863225446
ClinGen	rs863225446
ebi	rs863225446
HLI	rs863225446
Exac	rs863225446
Gnomad	rs863225446
Varsome	rs863225446
LitVar	rs863225446
Map	rs863225446
PheGenI	rs863225446
Biobank	rs863225446
1000 genomes	rs863225446
hgdp	rs863225446
ensembl	rs863225446
geneview	rs863225446
scholar	rs863225446
google	rs863225446
pharmgkb	rs863225446
gwascentral	rs863225446
openSNP	rs863225446
23andMe	rs863225446
SNPshot	rs863225446
SNPdbe	rs863225446
MSV3d	rs863225446
GWAS Ctlg	rs863225446

Max Magnitude

0

ClinVar
Risk	rs863225446(G;G)
Alt	rs863225446(G;G)
Reference	Rs863225446(A;A)
Significance	Pathogenic
Disease	Leigh syndrome
Variation	info
Gene	LRPPRC
CLNDBN	Leigh syndrome, French Canadian type
Reversed	1
HGVS	NC_000002.11:g.44187673T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000202398.2,