rs104893674

Orientation

plus

Stabilized

plus

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

Make rs104893674(A;A)

Make rs104893674(A;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

97737828

Gene

ZAP70

is a	snp
is	mentioned by
dbSNP	rs104893674
dbSNP (classic)	rs104893674
ClinGen	rs104893674
ebi	rs104893674
HLI	rs104893674
Exac	rs104893674
Gnomad	rs104893674
Varsome	rs104893674
LitVar	rs104893674
Map	rs104893674
PheGenI	rs104893674
Biobank	rs104893674
1000 genomes	rs104893674
hgdp	rs104893674
ensembl	rs104893674
geneview	rs104893674
scholar	rs104893674
google	rs104893674
pharmgkb	rs104893674
gwascentral	rs104893674
openSNP	rs104893674
23andMe	rs104893674
SNPshot	rs104893674
SNPdbe	rs104893674
MSV3d	rs104893674
GWAS Ctlg	rs104893674

Max Magnitude

0

OMIM	176947
Desc
Variant	0003
Related	also

ClinVar
Risk	rs104893674(A;A)
Alt	rs104893674(A;A)
Reference	Rs104893674(C;C)
Significance	Pathogenic
Disease	Severe combined immunodeficiency
Variation	info
Gene	ZAP70
CLNDBN	Severe combined immunodeficiency, atypical
Reversed	0
HGVS	NC_000002.11:g.98354291C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000033208.27,