rs863224871

Orientation

plus

Stabilized

plus

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

Make rs863224871(-;-)

Make rs863224871(-;AGCGAGC)

Make rs863224871(AGCGAGC;AGCGAGC)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

70203511

Gene

FADD

is a	snp
is	mentioned by
dbSNP	rs863224871
dbSNP (classic)	rs863224871
ClinGen	rs863224871
ebi	rs863224871
HLI	rs863224871
Exac	rs863224871
Gnomad	rs863224871
Varsome	rs863224871
LitVar	rs863224871
Map	rs863224871
PheGenI	rs863224871
Biobank	rs863224871
1000 genomes	rs863224871
hgdp	rs863224871
ensembl	rs863224871
geneview	rs863224871
scholar	rs863224871
google	rs863224871
pharmgkb	rs863224871
gwascentral	rs863224871
openSNP	rs863224871
23andMe	rs863224871
SNPshot	rs863224871
SNPdbe	rs863224871
MSV3d	rs863224871
GWAS Ctlg	rs863224871

Max Magnitude

0

ClinVar
Risk	rs863224871(-;-)
Alt	rs863224871(-;-)
Reference	Rs863224871(CGAGCAG;CGAGCAG)
Significance	Probable-Pathogenic
Disease	Infections
Variation	info
Gene	FADD
CLNDBN	Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations
Reversed	0
HGVS	NC_000011.9:g.70049617_70049623delAGCGAGC
CLNSRC
CLNACC	RCV000195419.1,