rs193922642

Orientation

plus

Stabilized

plus

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

Make rs193922642(A;C)

Make rs193922642(C;C)

Reference

GRCh38 38.1/141

Chromosome

5

Position

35873481

Gene

IL7R

is a	snp
is	mentioned by
dbSNP	rs193922642
dbSNP (classic)	rs193922642
ClinGen	rs193922642
ebi	rs193922642
HLI	rs193922642
Exac	rs193922642
Gnomad	rs193922642
Varsome	rs193922642
LitVar	rs193922642
Map	rs193922642
PheGenI	rs193922642
Biobank	rs193922642
1000 genomes	rs193922642
hgdp	rs193922642
ensembl	rs193922642
geneview	rs193922642
scholar	rs193922642
google	rs193922642
pharmgkb	rs193922642
gwascentral	rs193922642
openSNP	rs193922642
23andMe	rs193922642
SNPshot	rs193922642
SNPdbe	rs193922642
MSV3d	rs193922642
GWAS Ctlg	rs193922642

Max Magnitude

0

ClinVar
Risk	rs193922642(C;C)
Alt	rs193922642(C;C)
Reference	Rs193922642(A;A)
Significance	Probable-Pathogenic
Disease	Severe combined immunodeficiency disease
Variation	info
Gene	IL7R
CLNDBN	Severe combined immunodeficiency disease
Reversed	0
HGVS	NC_000005.9:g.35873583A>C
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030062.1,