rs587776807

Orientation

plus

Stabilized

plus

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

Make rs587776807(-;T)

Make rs587776807(T;T)

Reference

GRCh38 38.1/142

Chromosome

5

Position

159323098

Gene	IL12B, LOC107986469

is a	snp
is	mentioned by
dbSNP	rs587776807
dbSNP (classic)	rs587776807
ClinGen	rs587776807
ebi	rs587776807
HLI	rs587776807
Exac	rs587776807
Gnomad	rs587776807
Varsome	rs587776807
LitVar	rs587776807
Map	rs587776807
PheGenI	rs587776807
Biobank	rs587776807
1000 genomes	rs587776807
hgdp	rs587776807
ensembl	rs587776807
geneview	rs587776807
scholar	rs587776807
google	rs587776807
pharmgkb	rs587776807
gwascentral	rs587776807
openSNP	rs587776807
23andMe	rs587776807
SNPshot	rs587776807
SNPdbe	rs587776807
MSV3d	rs587776807
GWAS Ctlg	rs587776807

Max Magnitude

0

ClinVar
Risk	rs587776807(T;T)
Alt	rs587776807(T;T)
Reference	Rs587776807(-;-)
Significance	Pathogenic
Disease	Immunodeficiency 29
Variation	info
Gene	IL12B
CLNDBN	Immunodeficiency 29
Reversed	0
HGVS	NC_000005.9:g.158750106dupT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015098.27,