rs121913082

Orientation

plus

Stabilized

plus

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

Make rs121913082(A;G)

Make rs121913082(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

89014205

Gene

FAS

is a	snp
is	mentioned by
dbSNP	rs121913082
dbSNP (classic)	rs121913082
ClinGen	rs121913082
ebi	rs121913082
HLI	rs121913082
Exac	rs121913082
Gnomad	rs121913082
Varsome	rs121913082
LitVar	rs121913082
Map	rs121913082
PheGenI	rs121913082
Biobank	rs121913082
1000 genomes	rs121913082
hgdp	rs121913082
ensembl	rs121913082
geneview	rs121913082
scholar	rs121913082
google	rs121913082
pharmgkb	rs121913082
gwascentral	rs121913082
openSNP	rs121913082
23andMe	rs121913082
SNPshot	rs121913082
SNPdbe	rs121913082
MSV3d	rs121913082
GWAS Ctlg	rs121913082

Max Magnitude

0

OMIM	134637
Desc
Variant	0014
Related	also

ClinVar
Risk	rs121913082(G;G)
Alt	rs121913082(G;G)
Reference	Rs121913082(A;A)
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.90773962A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017974.5,