rs606231417

Orientation

plus

Stabilized

plus

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

Make rs606231417(C;T)

Make rs606231417(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

203870627

Gene

CTLA4

is a	snp
is	mentioned by
dbSNP	rs606231417
dbSNP (classic)	rs606231417
ClinGen	rs606231417
ebi	rs606231417
HLI	rs606231417
Exac	rs606231417
Gnomad	rs606231417
Varsome	rs606231417
LitVar	rs606231417
Map	rs606231417
PheGenI	rs606231417
Biobank	rs606231417
1000 genomes	rs606231417
hgdp	rs606231417
ensembl	rs606231417
geneview	rs606231417
scholar	rs606231417
google	rs606231417
pharmgkb	rs606231417
gwascentral	rs606231417
openSNP	rs606231417
23andMe	rs606231417
SNPshot	rs606231417
SNPdbe	rs606231417
MSV3d	rs606231417
GWAS Ctlg	rs606231417

Max Magnitude

0

ClinVar
Risk	rs606231417(T;T)
Alt	rs606231417(T;T)
Reference	Rs606231417(C;C)
Significance	Pathogenic
Disease	Autoimmune lymphoproliferatiVe syndrome
Variation	info
Gene	CTLA4
CLNDBN	Autoimmune lymphoproliferatiVe syndrome, type V
Reversed	0
HGVS	NC_000002.11:g.204735350C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000148290.2,