rs121913085

Orientation

plus

Stabilized

plus

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

Make rs121913085(C;C)

Make rs121913085(C;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

89014182

Gene

FAS

is a	snp
is	mentioned by
dbSNP	rs121913085
dbSNP (classic)	rs121913085
ClinGen	rs121913085
ebi	rs121913085
HLI	rs121913085
Exac	rs121913085
Gnomad	rs121913085
Varsome	rs121913085
LitVar	rs121913085
Map	rs121913085
PheGenI	rs121913085
Biobank	rs121913085
1000 genomes	rs121913085
hgdp	rs121913085
ensembl	rs121913085
geneview	rs121913085
scholar	rs121913085
google	rs121913085
pharmgkb	rs121913085
gwascentral	rs121913085
openSNP	rs121913085
23andMe	rs121913085
SNPshot	rs121913085
SNPdbe	rs121913085
MSV3d	rs121913085
GWAS Ctlg	rs121913085

Merged from

Rs28929499

Max Magnitude

0

OMIM	134637
Desc
Variant	0017
Related	also

ClinVar
Risk	rs121913085(C;C)
Alt	rs121913085(C;C)
Reference	Rs121913085(G;G)
Significance	Pathogenic
Disease	Autoimmune lymphoproliferative syndrome
Variation	info
Gene	FAS
CLNDBN	Autoimmune lymphoproliferative syndrome, type 1a
Reversed	0
HGVS	NC_000010.10:g.90773939G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017977.29,