rs11575933

Orientation

plus

Stabilized

plus

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

Make rs11575933(C;T)

Make rs11575933(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

133436943

Gene

ADAMTS13

is a	snp
is	mentioned by
dbSNP	rs11575933
dbSNP (classic)	rs11575933
ClinGen	rs11575933
ebi	rs11575933
HLI	rs11575933
Exac	rs11575933
Gnomad	rs11575933
Varsome	rs11575933
LitVar	rs11575933
Map	rs11575933
PheGenI	rs11575933
Biobank	rs11575933
1000 genomes	rs11575933
hgdp	rs11575933
ensembl	rs11575933
geneview	rs11575933
scholar	rs11575933
google	rs11575933
pharmgkb	rs11575933
gwascentral	rs11575933
openSNP	rs11575933
23andMe	rs11575933
SNPshot	rs11575933
SNPdbe	rs11575933
MSV3d	rs11575933
GWAS Ctlg	rs11575933

GMAF

0.009183

Max Magnitude

0

OMIM	604134
Desc
Variant	0016
Related	also

ClinVar
Risk	rs11575933(T;T)
Alt	rs11575933(T;T)
Reference	Rs11575933(C;C)
Significance	Other
Disease	Upshaw-Schulman syndrome not specified
Variation	info
Gene	ADAMTS13
CLNDBN	Upshaw-Schulman syndrome not specified
Reversed	0
HGVS	NC_000009.11:g.136302063C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006170.5, RCV000251648.1,