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rs768474112

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs768474112(A;A)
Make rs768474112(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position186273177
GeneF11
is asnp
is mentioned by
dbSNPrs768474112
ebirs768474112
HLIrs768474112
Exacrs768474112
Varsomers768474112
Maprs768474112
PheGenIrs768474112
hapmaprs768474112
1000 genomesrs768474112
hgdprs768474112
ensemblrs768474112
gopubmedrs768474112
geneviewrs768474112
scholarrs768474112
googlers768474112
pharmgkbrs768474112
gwascentralrs768474112
openSNPrs768474112
23andMers768474112
23andMe allrs768474112
SNP Nexus

SNPshotrs768474112
SNPdbers768474112
MSV3drs768474112
GWAS Ctlgrs768474112
Max Magnitude0
ClinVar
Risk rs768474112(A;A)
Alt rs768474112(A;A)
Reference rs768474112(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.187194331G>A
CLNSRC
CLNACC RCV000169144.1,