rs1801318

minus

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

Make rs1801318(A;G)

Make rs1801318(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

206141952

Gene

NDUFS1

is a	snp
is	mentioned by
dbSNP	rs1801318
dbSNP (classic)	rs1801318
ClinGen	rs1801318
ebi	rs1801318
HLI	rs1801318
Exac	rs1801318
Gnomad	rs1801318
Varsome	rs1801318
LitVar	rs1801318
Map	rs1801318
PheGenI	rs1801318
Biobank	rs1801318
1000 genomes	rs1801318
hgdp	rs1801318
ensembl	rs1801318
geneview	rs1801318
scholar	rs1801318
google	rs1801318
pharmgkb	rs1801318
gwascentral	rs1801318
openSNP	rs1801318
23andMe	rs1801318
SNPshot	rs1801318
SNPdbe	rs1801318
MSV3d	rs1801318
GWAS Ctlg	rs1801318

GMAF

0.3269

Max Magnitude

0

[PMID 24196945 ] A Hypothesis Driven Association Study of 28 Nuclear-Encoded Mitochondrial Genes With Antipsychotic-Induced Weight Gain in Schizophrenia

?

(A;A) (A;G) (G;G)

[PMID 16436204 ] GPNN: power studies and applications of a neural network method for detecting gene-gene interactions in studies of human disease.

ClinVar
Risk	rs1801318(G;G) rs1801318(T;T)
Alt	rs1801318(G;G) rs1801318(T;T)
Reference	Rs1801318(A;A)
Significance	Other
Disease	not specified Mitochondrial complex I deficiency Leigh syndrome
Variation	info
Gene	NDUFS1
CLNDBN	not specified Mitochondrial complex I deficiency Leigh syndrome
Reversed	1
HGVS	NC_000002.11:g.207006676T>C
CLNSRC	ClinVar University of Chicago
CLNACC	RCV000117709.3, RCV000301574.1, RCV000358690.1,