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rs41314453

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41314453(C;T)
Make rs41314453(T;T)
ReferenceGRCh38 38.1/142
Chromosome9
Position133442704
GeneADAMTS13
is asnp
is mentioned by
dbSNPrs41314453
ebirs41314453
HLIrs41314453
Exacrs41314453
Varsomers41314453
Maprs41314453
PheGenIrs41314453
hapmaprs41314453
1000 genomesrs41314453
hgdprs41314453
ensemblrs41314453
gopubmedrs41314453
geneviewrs41314453
scholarrs41314453
googlers41314453
pharmgkbrs41314453
gwascentralrs41314453
openSNPrs41314453
23andMers41314453
23andMe allrs41314453
SNP Nexus

SNPshotrs41314453
SNPdbers41314453
MSV3drs41314453
GWAS Ctlgrs41314453
Max Magnitude0

[PMID 25934476] Genetic variants in the ADAMTS13 and SUPT3H genes are associated with ADAMTS13 activity

ClinVar
Risk rs41314453(T;T)
Alt rs41314453(T;T)
Reference rs41314453(C;C)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene ADAMTS13
CLNDBN not specified
Reversed 0
HGVS NC_000009.11:g.136307825C>T
CLNSRC
CLNACC RCV000220213.1,