rs376722149

Orientation

plus

Stabilized

plus

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

Make rs376722149(C;T)

Make rs376722149(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

47584422

Gene

NDUFS3

is a	snp
is	mentioned by
dbSNP	rs376722149
dbSNP (classic)	rs376722149
ClinGen	rs376722149
ebi	rs376722149
HLI	rs376722149
Exac	rs376722149
Gnomad	rs376722149
Varsome	rs376722149
LitVar	rs376722149
Map	rs376722149
PheGenI	rs376722149
Biobank	rs376722149
1000 genomes	rs376722149
hgdp	rs376722149
ensembl	rs376722149
geneview	rs376722149
scholar	rs376722149
google	rs376722149
pharmgkb	rs376722149
gwascentral	rs376722149
openSNP	rs376722149
23andMe	rs376722149
SNPshot	rs376722149
SNPdbe	rs376722149
MSV3d	rs376722149
GWAS Ctlg	rs376722149

Max Magnitude

0

ClinVar
Risk	rs376722149(T;T)
Alt	rs376722149(T;T)
Reference	Rs376722149(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NDUFS3
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.47605974C>T
CLNSRC
CLNACC	RCV000198333.2,