rs587776858

Orientation

plus

Stabilized

plus

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

Make rs587776858(-;-)

Make rs587776858(-;CTT)

Reference

GRCh38 38.1/142

Chromosome

6

Position

137203577

Gene

IFNGR1

is a	snp
is	mentioned by
dbSNP	rs587776858
dbSNP (classic)	rs587776858
ClinGen	rs587776858
ebi	rs587776858
HLI	rs587776858
Exac	rs587776858
Gnomad	rs587776858
Varsome	rs587776858
LitVar	rs587776858
Map	rs587776858
PheGenI	rs587776858
Biobank	rs587776858
1000 genomes	rs587776858
hgdp	rs587776858
ensembl	rs587776858
geneview	rs587776858
scholar	rs587776858
google	rs587776858
pharmgkb	rs587776858
gwascentral	rs587776858
openSNP	rs587776858
23andMe	rs587776858
SNPshot	rs587776858
SNPdbe	rs587776858
MSV3d	rs587776858
GWAS Ctlg	rs587776858

Max Magnitude

0

ClinVar
Risk	rs587776858(-;-)
Alt	rs587776858(-;-)
Reference	Rs587776858(CTT;CTT)
Significance	Pathogenic
Disease	Disseminated atypical mycobacterial infection
Variation	info
Gene	IFNGR1
CLNDBN	Disseminated atypical mycobacterial infection
Reversed	0
HGVS	NC_000006.11:g.137524714_137524716delCTT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019547.31,