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

rs773905328

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs773905328(A;A)
Make rs773905328(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position186280552
GeneF11
is asnp
is mentioned by
dbSNPrs773905328
ebirs773905328
HLIrs773905328
Exacrs773905328
Varsomers773905328
Maprs773905328
PheGenIrs773905328
hapmaprs773905328
1000 genomesrs773905328
hgdprs773905328
ensemblrs773905328
gopubmedrs773905328
geneviewrs773905328
scholarrs773905328
googlers773905328
pharmgkbrs773905328
gwascentralrs773905328
openSNPrs773905328
23andMers773905328
23andMe allrs773905328
SNP Nexus

SNPshotrs773905328
SNPdbers773905328
MSV3drs773905328
GWAS Ctlgrs773905328
Max Magnitude0
ClinVar
Risk rs773905328(A;A)
Alt rs773905328(A;A)
Reference rs773905328(C;C)
Significance Probable-Pathogenic
Disease Hereditary factor XI deficiency disease
Variation info
Gene F11
CLNDBN Hereditary factor XI deficiency disease
Reversed 0
HGVS NC_000004.11:g.187201706C>A
CLNSRC
CLNACC RCV000169527.1,