Have questions? Visit https://www.reddit.com/r/SNPedia

rs121918667

From SNPedia

Orientationminus
Stabilizedminus
Make rs121918667(A;A)
Make rs121918667(A;G)
Make rs121918667(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position23049347
GeneTHBD
is asnp
is mentioned by
dbSNPrs121918667
ClinGenrs121918667
ebirs121918667
HLIrs121918667
Exacrs121918667
Varsomers121918667
Maprs121918667
PheGenIrs121918667
hapmaprs121918667
1000 genomesrs121918667
hgdprs121918667
ensemblrs121918667
gopubmedrs121918667
geneviewrs121918667
scholarrs121918667
googlers121918667
pharmgkbrs121918667
gwascentralrs121918667
openSNPrs121918667
23andMers121918667
23andMe allrs121918667
SNP Nexus

SNPshotrs121918667
SNPdbers121918667
MSV3drs121918667
GWAS Ctlgrs121918667
Max Magnitude
OMIM188040
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121918667(G;G)
Alt rs121918667(G;G)
Reference rs121918667(A;A)
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.23029984T>C
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000013556.3,