rs387906344

Orientation

plus

Stabilized

plus

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

Make rs387906344(-;-)

Make rs387906344(-;TT)

Reference

GRCh38 38.1/141

Chromosome

9

Position

133439443

Gene

ADAMTS13

is a	snp
is	mentioned by
dbSNP	rs387906344
dbSNP (classic)	rs387906344
ClinGen	rs387906344
ebi	rs387906344
HLI	rs387906344
Exac	rs387906344
Gnomad	rs387906344
Varsome	rs387906344
LitVar	rs387906344
Map	rs387906344
PheGenI	rs387906344
Biobank	rs387906344
1000 genomes	rs387906344
hgdp	rs387906344
ensembl	rs387906344
geneview	rs387906344
scholar	rs387906344
google	rs387906344
pharmgkb	rs387906344
gwascentral	rs387906344
openSNP	rs387906344
23andMe	rs387906344
SNPshot	rs387906344
SNPdbe	rs387906344
MSV3d	rs387906344
GWAS Ctlg	rs387906344

Max Magnitude

0

ClinVar
Risk	rs387906344(-;-)
Alt	rs387906344(-;-)
Reference	Rs387906344(TT;TT)
Significance	Pathogenic
Disease	Upshaw-Schulman syndrome
Variation	info
Gene	ADAMTS13
CLNDBN	Upshaw-Schulman syndrome
Reversed	0
HGVS	NC_000009.11:g.136304564_136304565delTT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006171.4,