rs137852616

Orientation

minus

Stabilized

minus

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

Make rs137852616(A;A)

Make rs137852616(A;G)

Reference

GRCh38 38.1/141

Chromosome

21

Position

44900367

Gene

ITGB2

is a	snp
is	mentioned by
dbSNP	rs137852616
dbSNP (classic)	rs137852616
ClinGen	rs137852616
ebi	rs137852616
HLI	rs137852616
Exac	rs137852616
Gnomad	rs137852616
Varsome	rs137852616
LitVar	rs137852616
Map	rs137852616
PheGenI	rs137852616
Biobank	rs137852616
1000 genomes	rs137852616
hgdp	rs137852616
ensembl	rs137852616
geneview	rs137852616
scholar	rs137852616
google	rs137852616
pharmgkb	rs137852616
gwascentral	rs137852616
openSNP	rs137852616
23andMe	rs137852616
SNPshot	rs137852616
SNPdbe	rs137852616
MSV3d	rs137852616
GWAS Ctlg	rs137852616

Max Magnitude

0

OMIM	600065
Desc
Variant	0012
Related	also

ClinVar
Risk	rs137852616(A;A)
Alt	rs137852616(A;A)
Reference	Rs137852616(G;G)
Significance	Other
Disease	Leukocyte adhesion deficiency
Variation	info
Gene	ITGB2
CLNDBN	Leukocyte adhesion deficiency
Reversed	1
HGVS	NC_000021.8:g.46320282C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010077.3,