rs886039596

Orientation

plus

Stabilized

plus

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

Make rs886039596(C;G)

Make rs886039596(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

85903024

Gene

IRF8

is a	snp
is	mentioned by
dbSNP	rs886039596
dbSNP (classic)	rs886039596
ClinGen	rs886039596
ebi	rs886039596
HLI	rs886039596
Exac	rs886039596
Gnomad	rs886039596
Varsome	rs886039596
LitVar	rs886039596
Map	rs886039596
PheGenI	rs886039596
Biobank	rs886039596
1000 genomes	rs886039596
hgdp	rs886039596
ensembl	rs886039596
geneview	rs886039596
scholar	rs886039596
google	rs886039596
pharmgkb	rs886039596
gwascentral	rs886039596
openSNP	rs886039596
23andMe	rs886039596
SNPshot	rs886039596
SNPdbe	rs886039596
MSV3d	rs886039596
GWAS Ctlg	rs886039596

Max Magnitude

0

ClinVar
Risk	rs886039596(G;G)
Alt	rs886039596(G;G)
Reference	Rs886039596(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	IRF8
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.85936630C>G
CLNSRC
CLNACC	RCV000255394.1,