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rs1057517364

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517364(A;A)
Make rs1057517364(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position186274115
GeneF11
is asnp
is mentioned by
dbSNPrs1057517364
dbSNP (old)rs1057517364
ClinGenrs1057517364
ebirs1057517364
HLIrs1057517364
Exacrs1057517364
Gnomadrs1057517364
Varsomers1057517364
Maprs1057517364
PheGenIrs1057517364
Biobankrs1057517364
1000 genomesrs1057517364
hgdprs1057517364
ensemblrs1057517364
gopubmedrs1057517364
geneviewrs1057517364
scholarrs1057517364
googlers1057517364
pharmgkbrs1057517364
gwascentralrs1057517364
openSNPrs1057517364
23andMers1057517364
23andMe allrs1057517364
SNPshotrs1057517364
SNPdbers1057517364
MSV3drs1057517364
GWAS Ctlgrs1057517364
Max Magnitude0
ClinVar
Risk rs1057517364(A;A)
Alt rs1057517364(A;A)
Reference Rs1057517364(G;G)
Significance Pathogenic
Disease Hereditary factor XI deficiency disease
Variation info
Gene F11
CLNDBN Hereditary factor XI deficiency disease
Reversed 0
HGVS NC_000004.11:g.187195269G>A
CLNSRC
CLNACC RCV000409991.1,