rs104894199

Orientation

plus

Stabilized

plus

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

Make rs104894199(A;G)

Make rs104894199(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

118344424

Gene	CD3D, CD3G

is a	snp
is	mentioned by
dbSNP	rs104894199
dbSNP (classic)	rs104894199
ClinGen	rs104894199
ebi	rs104894199
HLI	rs104894199
Exac	rs104894199
Gnomad	rs104894199
Varsome	rs104894199
LitVar	rs104894199
Map	rs104894199
PheGenI	rs104894199
Biobank	rs104894199
1000 genomes	rs104894199
hgdp	rs104894199
ensembl	rs104894199
geneview	rs104894199
scholar	rs104894199
google	rs104894199
pharmgkb	rs104894199
gwascentral	rs104894199
openSNP	rs104894199
23andMe	rs104894199
SNPshot	rs104894199
SNPdbe	rs104894199
MSV3d	rs104894199
GWAS Ctlg	rs104894199

Max Magnitude

0

OMIM	186740
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894199(G;G)
Alt	rs104894199(G;G)
Reference	Rs104894199(A;A)
Significance	Pathogenic
Disease	Immunodeficiency 17
Variation	info
Gene	CD3D CD3G
CLNDBN	Immunodeficiency 17
Reversed	0
HGVS	NC_000011.9:g.118215139A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000087021.3,