rs606231418

Orientation

plus

Stabilized

plus

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

Make rs606231418(-;-)

Make rs606231418(-;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

203868017

Gene

CTLA4

is a	snp
is	mentioned by
dbSNP	rs606231418
dbSNP (classic)	rs606231418
ClinGen	rs606231418
ebi	rs606231418
HLI	rs606231418
Exac	rs606231418
Gnomad	rs606231418
Varsome	rs606231418
LitVar	rs606231418
Map	rs606231418
PheGenI	rs606231418
Biobank	rs606231418
1000 genomes	rs606231418
hgdp	rs606231418
ensembl	rs606231418
geneview	rs606231418
scholar	rs606231418
google	rs606231418
pharmgkb	rs606231418
gwascentral	rs606231418
openSNP	rs606231418
23andMe	rs606231418
SNPshot	rs606231418
SNPdbe	rs606231418
MSV3d	rs606231418
GWAS Ctlg	rs606231418

Max Magnitude

0

ClinVar
Risk	rs606231418(-;-)
Alt	rs606231418(-;-)
Reference	Rs606231418(G;G)
Significance	Pathogenic
Disease	Autoimmune lymphoproliferatiVe syndrome
Variation	info
Gene	CTLA4
CLNDBN	Autoimmune lymphoproliferatiVe syndrome, type V
Reversed	0
HGVS	NC_000002.11:g.204732740delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000148291.2,