rs863225092

Orientation

minus

Stabilized

minus

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

Make rs863225092(C;T)

Make rs863225092(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

151811399

Gene

RORC

is a	snp
is	mentioned by
dbSNP	rs863225092
dbSNP (classic)	rs863225092
ClinGen	rs863225092
ebi	rs863225092
HLI	rs863225092
Exac	rs863225092
Gnomad	rs863225092
Varsome	rs863225092
LitVar	rs863225092
Map	rs863225092
PheGenI	rs863225092
Biobank	rs863225092
1000 genomes	rs863225092
hgdp	rs863225092
ensembl	rs863225092
geneview	rs863225092
scholar	rs863225092
google	rs863225092
pharmgkb	rs863225092
gwascentral	rs863225092
openSNP	rs863225092
23andMe	rs863225092
SNPshot	rs863225092
SNPdbe	rs863225092
MSV3d	rs863225092
GWAS Ctlg	rs863225092

Max Magnitude

0

ClinVar
Risk	rs863225092(T;T)
Alt	rs863225092(T;T)
Reference	Rs863225092(C;C)
Significance	Pathogenic
Disease	Immunodeficiency 42
Variation	info
Gene	RORC
CLNDBN	Immunodeficiency 42
Reversed	1
HGVS	NC_000001.10:g.151783875G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000201397.2,