rs886040870

Orientation

plus

Stabilized

plus

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

Make rs886040870(-;-)

Make rs886040870(-;CAAGAGGTGT)

Make rs886040870(CAAGAGGTGT;CAAGAGGTGT)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50776224

Gene

CYLD

is a	snp
is	mentioned by
dbSNP	rs886040870
dbSNP (classic)	rs886040870
ClinGen	rs886040870
ebi	rs886040870
HLI	rs886040870
Exac	rs886040870
Gnomad	rs886040870
Varsome	rs886040870
LitVar	rs886040870
Map	rs886040870
PheGenI	rs886040870
Biobank	rs886040870
1000 genomes	rs886040870
hgdp	rs886040870
ensembl	rs886040870
geneview	rs886040870
scholar	rs886040870
google	rs886040870
pharmgkb	rs886040870
gwascentral	rs886040870
openSNP	rs886040870
23andMe	rs886040870
SNPshot	rs886040870
SNPdbe	rs886040870
MSV3d	rs886040870
GWAS Ctlg	rs886040870

Max Magnitude

0

ClinVar
Risk	rs886040870(-;-)
Alt	rs886040870(-;-)
Reference	Rs886040870(TGTCAAGAGG;TGTCAAGAGG)
Significance	Pathogenic
Disease	Spiegler-Brooke syndrome
Variation	info
Gene	CYLD
CLNDBN	Spiegler-Brooke syndrome
Reversed	0
HGVS	NC_000016.9:g.50810135_50810144delCAAGAGGTGT
CLNSRC
CLNACC	RCV000257938.1,