rs2274064

Orientation

plus

Stabilized

plus

Make rs2274064(C;C)

Make rs2274064(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

183573252

Gene

NCF2

is a	snp
is	mentioned by
dbSNP	rs2274064
dbSNP (classic)	rs2274064
ClinGen	rs2274064
ebi	rs2274064
HLI	rs2274064
Exac	rs2274064
Gnomad	rs2274064
Varsome	rs2274064
LitVar	rs2274064
Map	rs2274064
PheGenI	rs2274064
Biobank	rs2274064
1000 genomes	rs2274064
hgdp	rs2274064
ensembl	rs2274064
geneview	rs2274064
scholar	rs2274064
google	rs2274064
pharmgkb	rs2274064
gwascentral	rs2274064
openSNP	rs2274064
23andMe	rs2274064
SNPshot	rs2274064
SNPdbe	rs2274064
MSV3d	rs2274064
GWAS Ctlg	rs2274064

Merged from

Rs34730753

GMAF

0.4977

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 16608528] Genetic polymorphisms and susceptibility to lung disease.

ClinVar
Risk	rs2274064(C;C)
Alt	rs2274064(C;C)
Reference	Rs2274064(T;T)
Significance	Non-pathogenic
Disease	not specified Chronic granulomatous disease
Variation	info
Gene	NCF2
CLNDBN	not specified Chronic granulomatous disease
Reversed	0
HGVS	NC_000001.10:g.183542387T>C
CLNSRC
CLNACC	RCV000243467.1, RCV000388595.1,