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rs886043418

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Chromosome4
Position109766801
GeneCFI
is asnp
is mentioned by
dbSNPrs886043418
dbSNP (classic)rs886043418
ClinGenrs886043418
ebirs886043418
HLIrs886043418
Exacrs886043418
Gnomadrs886043418
Varsomers886043418
LitVarrs886043418
Maprs886043418
PheGenIrs886043418
Biobankrs886043418
1000 genomesrs886043418
hgdprs886043418
ensemblrs886043418
geneviewrs886043418
scholarrs886043418
googlers886043418
pharmgkbrs886043418
gwascentralrs886043418
openSNPrs886043418
23andMers886043418
SNPshotrs886043418
SNPdbers886043418
MSV3drs886043418
GWAS Ctlgrs886043418
Max Magnitude0
ClinVar
Risk rs886043418(-;-)
Alt rs886043418(-;-)
Reference Rs886043418(AT;AT)
Significance Pathogenic
Disease Afibrinogenemia
Variation info
Gene CFI
CLNDBN Afibrinogenemia
Reversed 0
HGVS NC_000004.11:g.110687957_110687958delAT
CLNSRC
CLNACC RCV000375571.1,