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rs786204449

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs786204449(-;-)
Make rs786204449(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position186280318
GeneF11
is asnp
is mentioned by
dbSNPrs786204449
ebirs786204449
HLIrs786204449
Exacrs786204449
Varsomers786204449
Maprs786204449
PheGenIrs786204449
hapmaprs786204449
1000 genomesrs786204449
hgdprs786204449
ensemblrs786204449
gopubmedrs786204449
geneviewrs786204449
scholarrs786204449
googlers786204449
pharmgkbrs786204449
gwascentralrs786204449
openSNPrs786204449
23andMers786204449
23andMe allrs786204449
SNP Nexus

SNPshotrs786204449
SNPdbers786204449
MSV3drs786204449
GWAS Ctlgrs786204449
Max Magnitude0
ClinVar
Risk rs786204449(;)
Alt rs786204449(;)
Reference rs786204449(TG;TG)
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.187201472_187201473delTG
CLNSRC
CLNACC RCV000169073.1,