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rs145906668

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs145906668(C;T)
Make rs145906668(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position186288514
GeneF11, F11-AS1
is asnp
is mentioned by
dbSNPrs145906668
dbSNP (old)rs145906668
ClinGenrs145906668
ebirs145906668
HLIrs145906668
Exacrs145906668
Gnomadrs145906668
Varsomers145906668
Maprs145906668
PheGenIrs145906668
Biobankrs145906668
1000 genomesrs145906668
hgdprs145906668
ensemblrs145906668
gopubmedrs145906668
geneviewrs145906668
scholarrs145906668
googlers145906668
pharmgkbrs145906668
gwascentralrs145906668
openSNPrs145906668
23andMers145906668
23andMe allrs145906668
SNPshotrs145906668
SNPdbers145906668
MSV3drs145906668
GWAS Ctlgrs145906668
Max Magnitude0
ClinVar
Risk rs145906668(T;T)
Alt rs145906668(T;T)
Reference Rs145906668(C;C)
Significance Probable-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.187209668C>T
CLNSRC
CLNACC RCV000411281.1,