rs587776638

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(I;I)	0	common genotype
(T;T)	0	common in clinvar
(TC;TC)	0	common in clinvar

Make rs587776638(-;-)

Make rs587776638(-;A)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

85267901

Gene

BCL10

is a	snp
is	mentioned by
dbSNP	rs587776638
dbSNP (classic)	rs587776638
ClinGen	rs587776638
ebi	rs587776638
HLI	rs587776638
Exac	rs587776638
Gnomad	rs587776638
Varsome	rs587776638
LitVar	rs587776638
Map	rs587776638
PheGenI	rs587776638
Biobank	rs587776638
1000 genomes	rs587776638
hgdp	rs587776638
ensembl	rs587776638
geneview	rs587776638
scholar	rs587776638
google	rs587776638
pharmgkb	rs587776638
gwascentral	rs587776638
openSNP	rs587776638
23andMe	rs587776638
SNPshot	rs587776638
SNPdbe	rs587776638
MSV3d	rs587776638
GWAS Ctlg	rs587776638

Max Magnitude

0

ClinVar
Risk	Rs587776638(A;A) rs587776638(-;-)
Alt	Rs587776638(A;A) rs587776638(-;-)
Reference	Rs587776638(T;T)
Significance	Pathogenic
Disease	Sezary syndrome
Variation	info
Gene	BCL10
CLNDBN	Sezary syndrome
Reversed	1
HGVS	NC_000001.10:g.85733584delA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006638.5,