rs786205223

Orientation

minus

Stabilized

minus

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

Make rs786205223(G;G)

Make rs786205223(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

613215

Gene

IRF7

is a	snp
is	mentioned by
dbSNP	rs786205223
dbSNP (classic)	rs786205223
ClinGen	rs786205223
ebi	rs786205223
HLI	rs786205223
Exac	rs786205223
Gnomad	rs786205223
Varsome	rs786205223
LitVar	rs786205223
Map	rs786205223
PheGenI	rs786205223
Biobank	rs786205223
1000 genomes	rs786205223
hgdp	rs786205223
ensembl	rs786205223
geneview	rs786205223
scholar	rs786205223
google	rs786205223
pharmgkb	rs786205223
gwascentral	rs786205223
openSNP	rs786205223
23andMe	rs786205223
SNPshot	rs786205223
SNPdbe	rs786205223
MSV3d	rs786205223
GWAS Ctlg	rs786205223

Max Magnitude

0

ClinVar
Risk	rs786205223(G;G)
Alt	rs786205223(G;G)
Reference	Rs786205223(T;T)
Significance	Pathogenic
Disease	Immunodeficiency 39
Variation	info
Gene	IRF7
CLNDBN	Immunodeficiency 39
Reversed	1
HGVS	NC_000011.9:g.613215A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000170460.3,