rs111033581

Orientation

minus

Stabilized

minus

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

Make rs111033581(A;A)

Make rs111033581(A;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

118339902

Gene

CD3D

is a	snp
is	mentioned by
dbSNP	rs111033581
dbSNP (classic)	rs111033581
ClinGen	rs111033581
ebi	rs111033581
HLI	rs111033581
Exac	rs111033581
Gnomad	rs111033581
Varsome	rs111033581
LitVar	rs111033581
Map	rs111033581
PheGenI	rs111033581
Biobank	rs111033581
1000 genomes	rs111033581
hgdp	rs111033581
ensembl	rs111033581
geneview	rs111033581
scholar	rs111033581
google	rs111033581
pharmgkb	rs111033581
gwascentral	rs111033581
openSNP	rs111033581
23andMe	rs111033581
SNPshot	rs111033581
SNPdbe	rs111033581
MSV3d	rs111033581
GWAS Ctlg	rs111033581

Max Magnitude

0

OMIM	186790
Desc
Variant	0002
Related	also

ClinVar
Risk	rs111033581(A;A)
Alt	rs111033581(A;A)
Reference	Rs111033581(C;C)
Significance	Pathogenic
Disease	Immunodeficiency 19
Variation	info
Gene	CD3D
CLNDBN	Immunodeficiency 19
Reversed	1
HGVS	NC_000011.9:g.118210617G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000083295.3,