Have questions? Visit https://www.reddit.com/r/SNPedia

rs771896253

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs771896253(C;T)
Make rs771896253(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position186284142
GeneF11
is asnp
is mentioned by
dbSNPrs771896253
ebirs771896253
HLIrs771896253
Exacrs771896253
Varsomers771896253
Maprs771896253
PheGenIrs771896253
hapmaprs771896253
1000 genomesrs771896253
hgdprs771896253
ensemblrs771896253
gopubmedrs771896253
geneviewrs771896253
scholarrs771896253
googlers771896253
pharmgkbrs771896253
gwascentralrs771896253
openSNPrs771896253
23andMers771896253
23andMe allrs771896253
SNP Nexus

SNPshotrs771896253
SNPdbers771896253
MSV3drs771896253
GWAS Ctlgrs771896253
Max Magnitude0
ClinVar
Risk rs771896253(T;T)
Alt rs771896253(T;T)
Reference rs771896253(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.187205296C>T
CLNSRC
CLNACC RCV000169077.1,