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rs121964916

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964916(A;A)
Make rs121964916(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position109760567
GeneCFI
is asnp
is mentioned by
dbSNPrs121964916
ebirs121964916
HLIrs121964916
Exacrs121964916
Varsomers121964916
Maprs121964916
PheGenIrs121964916
hapmaprs121964916
1000 genomesrs121964916
hgdprs121964916
ensemblrs121964916
gopubmedrs121964916
geneviewrs121964916
scholarrs121964916
googlers121964916
pharmgkbrs121964916
gwascentralrs121964916
openSNPrs121964916
23andMers121964916
23andMe allrs121964916
SNP Nexus

SNPshotrs121964916
SNPdbers121964916
MSV3drs121964916
GWAS Ctlgrs121964916
Max Magnitude0
OMIM217030
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121964916(A;A)
Alt rs121964916(A;A)
Reference rs121964916(G;G)
Significance Pathogenic
Disease Afibrinogenemia
Variation info
Gene CFI
CLNDBN Afibrinogenemia
Reversed 1
HGVS NC_000004.11:g.110681723C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012907.22,