rs387906593

Orientation

minus

Stabilized

minus

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

Make rs387906593(A;A)

Make rs387906593(A;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

137219326

Gene

IFNGR1

is a	snp
is	mentioned by
dbSNP	rs387906593
dbSNP (classic)	rs387906593
ClinGen	rs387906593
ebi	rs387906593
HLI	rs387906593
Exac	rs387906593
Gnomad	rs387906593
Varsome	rs387906593
LitVar	rs387906593
Map	rs387906593
PheGenI	rs387906593
Biobank	rs387906593
1000 genomes	rs387906593
hgdp	rs387906593
ensembl	rs387906593
geneview	rs387906593
scholar	rs387906593
google	rs387906593
pharmgkb	rs387906593
gwascentral	rs387906593
openSNP	rs387906593
23andMe	rs387906593
SNPshot	rs387906593
SNPdbe	rs387906593
MSV3d	rs387906593
GWAS Ctlg	rs387906593

Max Magnitude

0

ClinVar
Risk	rs387906593(A;A) rs387906593(G;G)
Alt	rs387906593(A;A) rs387906593(G;G)
Reference	Rs387906593(T;T)
Significance	Pathogenic
Disease	Disseminated atypical mycobacterial infection
Variation	info
Gene	IFNGR1
CLNDBN	Disseminated atypical mycobacterial infection
Reversed	1
HGVS	NC_000006.11:g.137540463A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000022447.30,