rs587776822

Orientation

plus

Stabilized

plus

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

Make rs587776822(-;-)

Make rs587776822(-;AG)

Reference

GRCh38 38.1/142

Chromosome

21

Position

33421551

Gene

IFNGR2

is a	snp
is	mentioned by
dbSNP	rs587776822
dbSNP (classic)	rs587776822
ClinGen	rs587776822
ebi	rs587776822
HLI	rs587776822
Exac	rs587776822
Gnomad	rs587776822
Varsome	rs587776822
LitVar	rs587776822
Map	rs587776822
PheGenI	rs587776822
Biobank	rs587776822
1000 genomes	rs587776822
hgdp	rs587776822
ensembl	rs587776822
geneview	rs587776822
scholar	rs587776822
google	rs587776822
pharmgkb	rs587776822
gwascentral	rs587776822
openSNP	rs587776822
23andMe	rs587776822
SNPshot	rs587776822
SNPdbe	rs587776822
MSV3d	rs587776822
GWAS Ctlg	rs587776822

Max Magnitude

0

ClinVar
Risk	rs587776822(-;-)
Alt	rs587776822(-;-)
Reference	Rs587776822(AG;AG)
Significance	Pathogenic
Disease	Immunodeficiency 28
Variation	info
Gene	IFNGR2
CLNDBN	Immunodeficiency 28
Reversed	0
HGVS	NC_000021.8:g.34793858_34793859delAG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015847.27,