rs150667550

Orientation

plus

Stabilized

plus

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

Make rs150667550(C;C)

Make rs150667550(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

161210599

Gene

NDUFS2

is a	snp
is	mentioned by
dbSNP	rs150667550
dbSNP (classic)	rs150667550
ClinGen	rs150667550
ebi	rs150667550
HLI	rs150667550
Exac	rs150667550
Gnomad	rs150667550
Varsome	rs150667550
LitVar	rs150667550
Map	rs150667550
PheGenI	rs150667550
Biobank	rs150667550
1000 genomes	rs150667550
hgdp	rs150667550
ensembl	rs150667550
geneview	rs150667550
scholar	rs150667550
google	rs150667550
pharmgkb	rs150667550
gwascentral	rs150667550
openSNP	rs150667550
23andMe	rs150667550
SNPshot	rs150667550
SNPdbe	rs150667550
MSV3d	rs150667550
GWAS Ctlg	rs150667550

Max Magnitude

0

ClinVar
Risk	rs150667550(C;C)
Alt	rs150667550(C;C)
Reference	Rs150667550(T;T)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	NDUFS2
CLNDBN	not specified
Reversed	0
HGVS	NC_000001.10:g.161180389T>C
CLNSRC
CLNACC	RCV000198967.3,