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rs1057517151

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517151(-;-)
Make rs1057517151(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position186273143
GeneF11
is asnp
is mentioned by
dbSNPrs1057517151
dbSNP (old)rs1057517151
ClinGenrs1057517151
ebirs1057517151
HLIrs1057517151
Exacrs1057517151
Gnomadrs1057517151
Varsomers1057517151
Maprs1057517151
PheGenIrs1057517151
Biobankrs1057517151
1000 genomesrs1057517151
hgdprs1057517151
ensemblrs1057517151
gopubmedrs1057517151
geneviewrs1057517151
scholarrs1057517151
googlers1057517151
pharmgkbrs1057517151
gwascentralrs1057517151
openSNPrs1057517151
23andMers1057517151
23andMe allrs1057517151
SNP Nexus

SNPshotrs1057517151
SNPdbers1057517151
MSV3drs1057517151
GWAS Ctlgrs1057517151
Max Magnitude0
ClinVar
Risk rs1057517151(-;-)
Alt rs1057517151(-;-)
Reference Rs1057517151(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.187194297delG
CLNSRC
CLNACC RCV000409581.1,