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rs1057516738

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516738(A;A)
Make rs1057516738(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position186271772
GeneF11
is asnp
is mentioned by
dbSNPrs1057516738
dbSNP (old)rs1057516738
ClinGenrs1057516738
ebirs1057516738
HLIrs1057516738
Exacrs1057516738
Gnomadrs1057516738
Varsomers1057516738
Maprs1057516738
PheGenIrs1057516738
Biobankrs1057516738
1000 genomesrs1057516738
hgdprs1057516738
ensemblrs1057516738
gopubmedrs1057516738
geneviewrs1057516738
scholarrs1057516738
googlers1057516738
pharmgkbrs1057516738
gwascentralrs1057516738
openSNPrs1057516738
23andMers1057516738
23andMe allrs1057516738
SNP Nexus

SNPshotrs1057516738
SNPdbers1057516738
MSV3drs1057516738
GWAS Ctlgrs1057516738
Max Magnitude0
ClinVar
Risk rs1057516738(A;A)
Alt rs1057516738(A;A)
Reference Rs1057516738(G;G)
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.187192926G>A
CLNSRC
CLNACC RCV000409767.1,