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rs768409400

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768409400(C;T)
Make rs768409400(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position186271620
GeneF11
is asnp
is mentioned by
dbSNPrs768409400
ebirs768409400
HLIrs768409400
Exacrs768409400
Varsomers768409400
Maprs768409400
PheGenIrs768409400
hapmaprs768409400
1000 genomesrs768409400
hgdprs768409400
ensemblrs768409400
gopubmedrs768409400
geneviewrs768409400
scholarrs768409400
googlers768409400
pharmgkbrs768409400
gwascentralrs768409400
openSNPrs768409400
23andMers768409400
23andMe allrs768409400
SNP Nexus

SNPshotrs768409400
SNPdbers768409400
MSV3drs768409400
GWAS Ctlgrs768409400
Max Magnitude0
ClinVar
Risk rs768409400(T;T)
Alt rs768409400(T;T)
Reference rs768409400(C;C)
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.187192774C>T
CLNSRC
CLNACC RCV000169536.1,