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rs754087775

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs754087775(C;T)
Make rs754087775(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position186276386
GeneF11
is asnp
is mentioned by
dbSNPrs754087775
ebirs754087775
HLIrs754087775
Exacrs754087775
Varsomers754087775
Maprs754087775
PheGenIrs754087775
hapmaprs754087775
1000 genomesrs754087775
hgdprs754087775
ensemblrs754087775
gopubmedrs754087775
geneviewrs754087775
scholarrs754087775
googlers754087775
pharmgkbrs754087775
gwascentralrs754087775
openSNPrs754087775
23andMers754087775
23andMe allrs754087775
SNP Nexus

SNPshotrs754087775
SNPdbers754087775
MSV3drs754087775
GWAS Ctlgrs754087775
Max Magnitude0
ClinVar
Risk rs754087775(T;T)
Alt rs754087775(T;T)
Reference rs754087775(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.187197540C>T
CLNSRC
CLNACC RCV000169287.1,