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rs1057520680

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520680(A;A)
Make rs1057520680(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position133449966
GeneADAMTS13
is asnp
is mentioned by
dbSNPrs1057520680
dbSNP (old)rs1057520680
ClinGenrs1057520680
ebirs1057520680
HLIrs1057520680
Exacrs1057520680
Gnomadrs1057520680
Varsomers1057520680
Maprs1057520680
PheGenIrs1057520680
Biobankrs1057520680
1000 genomesrs1057520680
hgdprs1057520680
ensemblrs1057520680
gopubmedrs1057520680
geneviewrs1057520680
scholarrs1057520680
googlers1057520680
pharmgkbrs1057520680
gwascentralrs1057520680
openSNPrs1057520680
23andMers1057520680
23andMe allrs1057520680
SNPshotrs1057520680
SNPdbers1057520680
MSV3drs1057520680
GWAS Ctlgrs1057520680
Max Magnitude0
ClinVar
Risk rs1057520680(A;A)
Alt rs1057520680(A;A)
Reference Rs1057520680(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ADAMTS13
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.136315087G>A
CLNSRC
CLNACC RCV000435056.1,