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rs1800578

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1800578(C;T)
Make rs1800578(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position23048022
GeneTHBD
is asnp
is mentioned by
dbSNPrs1800578
ebirs1800578
HLIrs1800578
Exacrs1800578
Varsomers1800578
Maprs1800578
PheGenIrs1800578
hapmaprs1800578
1000 genomesrs1800578
hgdprs1800578
ensemblrs1800578
gopubmedrs1800578
geneviewrs1800578
scholarrs1800578
googlers1800578
pharmgkbrs1800578
gwascentralrs1800578
openSNPrs1800578
23andMers1800578
23andMe allrs1800578
SNP Nexus

SNPshotrs1800578
SNPdbers1800578
MSV3drs1800578
GWAS Ctlgrs1800578
Max Magnitude0
OMIM188040
Desc
Variant0007
Relatedalso


ClinVar
Risk rs1800578(T;T)
Alt rs1800578(T;T)
Reference rs1800578(C;C)
Significance Other
Disease Atypical hemolytic-uremic syndrome 6
Variation info
Gene THBD
CLNDBN Atypical hemolytic-uremic syndrome 6
Reversed 1
HGVS NC_000020.10:g.23028659G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013557.2,



[PMID 17677000OA-icon.png] Combined effects of thrombosis pathway gene variants predict cardiovascular events.