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rs398122807

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122807(G;T)
Make rs398122807(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position23048296
GeneTHBD
is asnp
is mentioned by
dbSNPrs398122807
ebirs398122807
HLIrs398122807
Exacrs398122807
Varsomers398122807
Maprs398122807
PheGenIrs398122807
hapmaprs398122807
1000 genomesrs398122807
hgdprs398122807
ensemblrs398122807
gopubmedrs398122807
geneviewrs398122807
scholarrs398122807
googlers398122807
pharmgkbrs398122807
gwascentralrs398122807
openSNPrs398122807
23andMers398122807
23andMe allrs398122807
SNP Nexus

SNPshotrs398122807
SNPdbers398122807
MSV3drs398122807
GWAS Ctlgrs398122807
Max Magnitude0
ClinVar
Risk rs398122807(T;T)
Alt rs398122807(T;T)
Reference rs398122807(G;G)
Significance Pathogenic
Disease Thrombophilia due to thrombomodulin defect
Variation info
Gene THBD
CLNDBN Thrombophilia due to thrombomodulin defect
Reversed 1
HGVS NC_000020.10:g.23028933C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022787.24,