rs193922573

Orientation

minus

Stabilized

minus

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

Make rs193922573(A;A)

Make rs193922573(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

36592860

Gene	C11orf74, RAG2

is a	snp
is	mentioned by
dbSNP	rs193922573
dbSNP (classic)	rs193922573
ClinGen	rs193922573
ebi	rs193922573
HLI	rs193922573
Exac	rs193922573
Gnomad	rs193922573
Varsome	rs193922573
LitVar	rs193922573
Map	rs193922573
PheGenI	rs193922573
Biobank	rs193922573
1000 genomes	rs193922573
hgdp	rs193922573
ensembl	rs193922573
geneview	rs193922573
scholar	rs193922573
google	rs193922573
pharmgkb	rs193922573
gwascentral	rs193922573
openSNP	rs193922573
23andMe	rs193922573
SNPshot	rs193922573
SNPdbe	rs193922573
MSV3d	rs193922573
GWAS Ctlg	rs193922573

Max Magnitude

0

ClinVar
Risk	rs193922573(A;A)
Alt	rs193922573(A;A)
Reference	Rs193922573(G;G)
Significance	Probable-Pathogenic
Disease	Severe combined immunodeficiency disease not provided
Variation	info
Gene	RAG2 C11orf74
CLNDBN	Severe combined immunodeficiency disease not provided
Reversed	1
HGVS	NC_000011.9:g.36614410C>T
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030397.1, RCV000413563.1,