rs387906341

Orientation

plus

Stabilized

plus

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

Make rs387906341(-;T)

Make rs387906341(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

133456597

Gene

ADAMTS13

is a	snp
is	mentioned by
dbSNP	rs387906341
dbSNP (classic)	rs387906341
ClinGen	rs387906341
ebi	rs387906341
HLI	rs387906341
Exac	rs387906341
Gnomad	rs387906341
Varsome	rs387906341
LitVar	rs387906341
Map	rs387906341
PheGenI	rs387906341
Biobank	rs387906341
1000 genomes	rs387906341
hgdp	rs387906341
ensembl	rs387906341
geneview	rs387906341
scholar	rs387906341
google	rs387906341
pharmgkb	rs387906341
gwascentral	rs387906341
openSNP	rs387906341
23andMe	rs387906341
SNPshot	rs387906341
SNPdbe	rs387906341
MSV3d	rs387906341
GWAS Ctlg	rs387906341

Max Magnitude

0

ClinVar
Risk	rs387906341(T;T)
Alt	rs387906341(T;T)
Reference	Rs387906341(-;-)
Significance	Pathogenic
Disease	Upshaw-Schulman syndrome
Variation	info
Gene	ADAMTS13
CLNDBN	Upshaw-Schulman syndrome
Reversed	0
HGVS	NC_000009.11:g.136321719dupT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006161.4,