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rs1057516506

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516506(G;T)
Make rs1057516506(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position186286414
GeneF11, F11-AS1
is asnp
is mentioned by
dbSNPrs1057516506
dbSNP (old)rs1057516506
ClinGenrs1057516506
ebirs1057516506
HLIrs1057516506
Exacrs1057516506
Gnomadrs1057516506
Varsomers1057516506
Maprs1057516506
PheGenIrs1057516506
Biobankrs1057516506
1000 genomesrs1057516506
hgdprs1057516506
ensemblrs1057516506
gopubmedrs1057516506
geneviewrs1057516506
scholarrs1057516506
googlers1057516506
pharmgkbrs1057516506
gwascentralrs1057516506
openSNPrs1057516506
23andMers1057516506
23andMe allrs1057516506
SNPshotrs1057516506
SNPdbers1057516506
MSV3drs1057516506
GWAS Ctlgrs1057516506
Max Magnitude0
ClinVar
Risk rs1057516506(T;T)
Alt rs1057516506(T;T)
Reference Rs1057516506(G;G)
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.187207568G>T
CLNSRC
CLNACC RCV000412477.1,