rs121913077

Orientation

plus

Stabilized

plus

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

Make rs121913077(C;T)

Make rs121913077(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

89014259

Gene

FAS

is a	snp
is	mentioned by
dbSNP	rs121913077
dbSNP (classic)	rs121913077
ClinGen	rs121913077
ebi	rs121913077
HLI	rs121913077
Exac	rs121913077
Gnomad	rs121913077
Varsome	rs121913077
LitVar	rs121913077
Map	rs121913077
PheGenI	rs121913077
Biobank	rs121913077
1000 genomes	rs121913077
hgdp	rs121913077
ensembl	rs121913077
geneview	rs121913077
scholar	rs121913077
google	rs121913077
pharmgkb	rs121913077
gwascentral	rs121913077
openSNP	rs121913077
23andMe	rs121913077
SNPshot	rs121913077
SNPdbe	rs121913077
MSV3d	rs121913077
GWAS Ctlg	rs121913077

Max Magnitude

0

OMIM	134637
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121913077(T;T)
Alt	rs121913077(T;T)
Reference	Rs121913077(C;C)
Significance	Pathogenic
Disease	Autoimmune lymphoproliferative syndrome
Variation	info
Gene	FAS
CLNDBN	Autoimmune lymphoproliferative syndrome, type 1a
Reversed	0
HGVS	NC_000010.10:g.90774016C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017965.29,