rs121913076

Orientation

plus

Stabilized

plus

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

Make rs121913076(A;C)

Make rs121913076(C;C)

Reference

GRCh38 38.1/141

Chromosome

10

Position

89014163

Gene

FAS

is a	snp
is	mentioned by
dbSNP	rs121913076
dbSNP (classic)	rs121913076
ClinGen	rs121913076
ebi	rs121913076
HLI	rs121913076
Exac	rs121913076
Gnomad	rs121913076
Varsome	rs121913076
LitVar	rs121913076
Map	rs121913076
PheGenI	rs121913076
Biobank	rs121913076
1000 genomes	rs121913076
hgdp	rs121913076
ensembl	rs121913076
geneview	rs121913076
scholar	rs121913076
google	rs121913076
pharmgkb	rs121913076
gwascentral	rs121913076
openSNP	rs121913076
23andMe	rs121913076
SNPshot	rs121913076
SNPdbe	rs121913076
MSV3d	rs121913076
GWAS Ctlg	rs121913076

Max Magnitude

0

OMIM	134637
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121913076(C;C)
Alt	rs121913076(C;C)
Reference	Rs121913076(A;A)
Significance	Pathogenic
Disease	Autoimmune lymphoproliferative syndrome
Variation	info
Gene	FAS
CLNDBN	Autoimmune lymphoproliferative syndrome, type 1a
Reversed	0
HGVS	NC_000010.10:g.90773920A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017963.29,