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rs121908470

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121908470(C;T)
Make rs121908470(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position133426246
GeneADAMTS13
is asnp
is mentioned by
dbSNPrs121908470
ebirs121908470
HLIrs121908470
Exacrs121908470
Varsomers121908470
Maprs121908470
PheGenIrs121908470
hapmaprs121908470
1000 genomesrs121908470
hgdprs121908470
ensemblrs121908470
gopubmedrs121908470
geneviewrs121908470
scholarrs121908470
googlers121908470
pharmgkbrs121908470
gwascentralrs121908470
openSNPrs121908470
23andMers121908470
23andMe allrs121908470
SNP Nexus

SNPshotrs121908470
SNPdbers121908470
MSV3drs121908470
GWAS Ctlgrs121908470
Max Magnitude0
OMIM604134
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121908470(T;T)
Alt rs121908470(T;T)
Reference rs121908470(C;C)
Significance Pathogenic
Disease Upshaw-Schulman syndrome
Variation info
Gene ADAMTS13
CLNDBN Upshaw-Schulman syndrome
Reversed 0
HGVS NC_000009.11:g.136291366C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006157.4,