rs7749390

plus

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

Make rs7749390(A;G)

Make rs7749390(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

137219233

Gene

IFNGR1

is a	snp
is	mentioned by
dbSNP	rs7749390
dbSNP (classic)	rs7749390
ClinGen	rs7749390
ebi	rs7749390
HLI	rs7749390
Exac	rs7749390
Gnomad	rs7749390
Varsome	rs7749390
LitVar	rs7749390
Map	rs7749390
PheGenI	rs7749390
Biobank	rs7749390
1000 genomes	rs7749390
hgdp	rs7749390
ensembl	rs7749390
geneview	rs7749390
scholar	rs7749390
google	rs7749390
pharmgkb	rs7749390
gwascentral	rs7749390
openSNP	rs7749390
23andMe	rs7749390
SNPshot	rs7749390
SNPdbe	rs7749390
MSV3d	rs7749390
GWAS Ctlg	rs7749390

GMAF

0.4458

Max Magnitude

0

?

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

28

[PMID 20500698] Analysis of functional SNP in ifng/ifngr1 in Chinese Han population with tuberculosis

[PMID 20412699] Lack of association between IFNGR1 gene polymorphisms and biopsy-proven giant cell arteritis

[PMID 17136124 ] IFNG and IFNGR1 gene polymorphisms and susceptibility to post-kala-azar dermal leishmaniasis in Sudan.

[PMID 21458658 ] Human atopic dermatitis complicated by eczema herpeticum is associated with abnormalities in IFN-gamma response.

ClinVar
Risk	rs7749390(G;G)
Alt	rs7749390(G;G)
Reference	Rs7749390(A;A)
Significance	Non-pathogenic
Disease	Familial Atypical Mycobacteriosis not specified
Variation	info
Gene	IFNGR1
CLNDBN	Familial Atypical Mycobacteriosis, Autosomal Recessive not specified
Reversed	0
HGVS	NC_000006.11:g.137540370A>G
CLNSRC
CLNACC	RCV000285373.1, RCV000455036.1,

[PMID 30100739 ] Polymorphism of IFN-γ +874T/A associated with production of IFN-γ affects human papillomavirus susceptibility in rural women from Luohe, Henan, China.