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rs121964912

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121964912(A;T)
Make rs121964912(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position109746398
GeneCFI
is asnp
is mentioned by
dbSNPrs121964912
ebirs121964912
HLIrs121964912
Exacrs121964912
Varsomers121964912
Maprs121964912
PheGenIrs121964912
hapmaprs121964912
1000 genomesrs121964912
hgdprs121964912
ensemblrs121964912
gopubmedrs121964912
geneviewrs121964912
scholarrs121964912
googlers121964912
pharmgkbrs121964912
gwascentralrs121964912
openSNPrs121964912
23andMers121964912
23andMe allrs121964912
SNP Nexus

SNPshotrs121964912
SNPdbers121964912
MSV3drs121964912
GWAS Ctlgrs121964912
Max Magnitude0
OMIM217030
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121964912(T;T)
Alt rs121964912(T;T)
Reference rs121964912(A;A)
Significance Pathogenic
Disease Afibrinogenemia
Variation info
Gene CFI
CLNDBN Afibrinogenemia
Reversed 1
HGVS NC_000004.11:g.110667554T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012901.16,