rs104893973

Orientation

minus

Stabilized

minus

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

Make rs104893973(C;C)

Make rs104893973(C;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

137206249

Gene

IFNGR1

is a	snp
is	mentioned by
dbSNP	rs104893973
dbSNP (classic)	rs104893973
ClinGen	rs104893973
ebi	rs104893973
HLI	rs104893973
Exac	rs104893973
Gnomad	rs104893973
Varsome	rs104893973
LitVar	rs104893973
Map	rs104893973
PheGenI	rs104893973
Biobank	rs104893973
1000 genomes	rs104893973
hgdp	rs104893973
ensembl	rs104893973
geneview	rs104893973
scholar	rs104893973
google	rs104893973
pharmgkb	rs104893973
gwascentral	rs104893973
openSNP	rs104893973
23andMe	rs104893973
SNPshot	rs104893973
SNPdbe	rs104893973
MSV3d	rs104893973
GWAS Ctlg	rs104893973

Max Magnitude

0

OMIM	107470
Desc
Variant	0003
Related	also

ClinVar
Risk	rs104893973(C;C)
Alt	rs104893973(C;C)
Reference	Rs104893973(T;T)
Significance	Other
Disease	Disseminated atypical mycobacterial infection Mycobacterium tuberculosis
Variation	info
Gene	IFNGR1
CLNDBN	Disseminated atypical mycobacterial infection Mycobacterium tuberculosis, susceptibility to
Reversed	1
HGVS	NC_000006.11:g.137527386A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019539.30, RCV000144034.3,