rs121913084

Orientation

plus

Stabilized

plus

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

Make rs121913084(C;C)

Make rs121913084(C;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

89010779

Gene

FAS

is a	snp
is	mentioned by
dbSNP	rs121913084
dbSNP (classic)	rs121913084
ClinGen	rs121913084
ebi	rs121913084
HLI	rs121913084
Exac	rs121913084
Gnomad	rs121913084
Varsome	rs121913084
LitVar	rs121913084
Map	rs121913084
PheGenI	rs121913084
Biobank	rs121913084
1000 genomes	rs121913084
hgdp	rs121913084
ensembl	rs121913084
geneview	rs121913084
scholar	rs121913084
google	rs121913084
pharmgkb	rs121913084
gwascentral	rs121913084
openSNP	rs121913084
23andMe	rs121913084
SNPshot	rs121913084
SNPdbe	rs121913084
MSV3d	rs121913084
GWAS Ctlg	rs121913084

Max Magnitude

0

OMIM	134637
Desc
Variant	0016
Related	also

ClinVar
Risk	rs121913084(C;C)
Alt	rs121913084(C;C)
Reference	Rs121913084(T;T)
Significance	Pathogenic
Disease	SQUAMOUS CELL CARCINOMA
Variation	info
Gene	FAS
CLNDBN	SQUAMOUS CELL CARCINOMA, BURN SCAR-RELATED, SOMATIC
Reversed	0
HGVS	NC_000010.10:g.90770536T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017976.5,