rs200890363

Orientation

plus

Stabilized

plus

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

Make rs200890363(A;G)

Make rs200890363(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

12397

Gene

ND5

is a	snp
is	mentioned by
dbSNP	rs200890363
dbSNP (classic)	rs200890363
ClinGen	rs200890363
ebi	rs200890363
HLI	rs200890363
Exac	rs200890363
Gnomad	rs200890363
Varsome	rs200890363
LitVar	rs200890363
Map	rs200890363
PheGenI	rs200890363
Biobank	rs200890363
1000 genomes	rs200890363
hgdp	rs200890363
ensembl	rs200890363
geneview	rs200890363
scholar	rs200890363
google	rs200890363
pharmgkb	rs200890363
gwascentral	rs200890363
openSNP	rs200890363
23andMe	rs200890363
SNPshot	rs200890363
SNPdbe	rs200890363
MSV3d	rs200890363
GWAS Ctlg	rs200890363

GMAF

0.003742

Max Magnitude

0

ClinVar
Risk	rs200890363(G;G)
Alt	rs200890363(G;G)
Reference	Rs200890363(A;A)
Significance	Other
Disease	Parkinson disease 6
Variation	info
Gene	ND5
CLNDBN	Parkinson disease 6, autosomal recessive early-onset
Reversed	0
HGVS	NC_012920.1:m.12397A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010351.3,