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rs28934609

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28934609(A;A)
Make rs28934609(A;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position186288518
GeneF11, PRAMEF4
is asnp
is mentioned by
dbSNPrs28934609
ebirs28934609
HLIrs28934609
Exacrs28934609
Varsomers28934609
Maprs28934609
PheGenIrs28934609
hapmaprs28934609
1000 genomesrs28934609
hgdprs28934609
ensemblrs28934609
gopubmedrs28934609
geneviewrs28934609
scholarrs28934609
googlers28934609
pharmgkbrs28934609
gwascentralrs28934609
openSNPrs28934609
23andMers28934609
23andMe allrs28934609
SNP Nexus

SNPshotrs28934609
SNPdbers28934609
MSV3drs28934609
GWAS Ctlgrs28934609
Max Magnitude0
OMIM264900
DescFACTOR XI DEFICIENCY
Variant0011
Relatedalso


ClinVar
Risk rs28934609(A;A)
Alt rs28934609(A;A)
Reference rs28934609(C;C)
Significance Pathogenic
Disease Hereditary factor XI deficiency disease
Variation info
Gene F11-AS1 F11
CLNDBN Hereditary factor XI deficiency disease
Reversed 0
HGVS NC_000004.11:g.187209672C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012675.18,