rs606231366

Orientation

plus

Stabilized

plus

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

Make rs606231366(-;T)

Make rs606231366(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

89014134

Gene

FAS

is a	snp
is	mentioned by
dbSNP	rs606231366
dbSNP (classic)	rs606231366
ClinGen	rs606231366
ebi	rs606231366
HLI	rs606231366
Exac	rs606231366
Gnomad	rs606231366
Varsome	rs606231366
LitVar	rs606231366
Map	rs606231366
PheGenI	rs606231366
Biobank	rs606231366
1000 genomes	rs606231366
hgdp	rs606231366
ensembl	rs606231366
geneview	rs606231366
scholar	rs606231366
google	rs606231366
pharmgkb	rs606231366
gwascentral	rs606231366
openSNP	rs606231366
23andMe	rs606231366
SNPshot	rs606231366
SNPdbe	rs606231366
MSV3d	rs606231366
GWAS Ctlg	rs606231366

Max Magnitude

0

ClinVar
Risk	rs606231366(T;T)
Alt	rs606231366(T;T)
Reference	Rs606231366(-;-)
Significance	Pathogenic
Disease	Autoimmune lymphoproliferative syndrome
Variation	info
Gene	FAS
CLNDBN	Autoimmune lymphoproliferative syndrome, type 1a
Reversed	0
HGVS	NC_000010.10:g.90773891_90773892insT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017979.29,