rs200387097

Orientation

plus

Stabilized

plus

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

Make rs200387097(C;T)

Make rs200387097(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

240014786

Gene

NDUFA10

is a	snp
is	mentioned by
dbSNP	rs200387097
dbSNP (classic)	rs200387097
ClinGen	rs200387097
ebi	rs200387097
HLI	rs200387097
Exac	rs200387097
Gnomad	rs200387097
Varsome	rs200387097
LitVar	rs200387097
Map	rs200387097
PheGenI	rs200387097
Biobank	rs200387097
1000 genomes	rs200387097
hgdp	rs200387097
ensembl	rs200387097
geneview	rs200387097
scholar	rs200387097
google	rs200387097
pharmgkb	rs200387097
gwascentral	rs200387097
openSNP	rs200387097
23andMe	rs200387097
SNPshot	rs200387097
SNPdbe	rs200387097
MSV3d	rs200387097
GWAS Ctlg	rs200387097

Max Magnitude

0

ClinVar
Risk	rs200387097(G;G) rs200387097(T;T)
Alt	rs200387097(G;G) rs200387097(T;T)
Reference	Rs200387097(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NDUFA10
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.240954203C>G
CLNSRC
CLNACC	RCV000198629.1,