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rs281875275

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281875275(A;A)
Make rs281875275(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position186287800
GeneF11, F11-AS1
is asnp
is mentioned by
dbSNPrs281875275
ebirs281875275
HLIrs281875275
Exacrs281875275
Varsomers281875275
Maprs281875275
PheGenIrs281875275
hapmaprs281875275
1000 genomesrs281875275
hgdprs281875275
ensemblrs281875275
gopubmedrs281875275
geneviewrs281875275
scholarrs281875275
googlers281875275
pharmgkbrs281875275
gwascentralrs281875275
openSNPrs281875275
23andMers281875275
23andMe allrs281875275
SNP Nexus

SNPshotrs281875275
SNPdbers281875275
MSV3drs281875275
GWAS Ctlgrs281875275
Max Magnitude0
ClinVar
Risk rs281875275(A;A)
Alt rs281875275(A;A)
Reference rs281875275(G;G)
Significance Probable-Pathogenic
Disease not provided Hereditary factor XI deficiency disease
Variation info
Gene F11-AS1 F11
CLNDBN not provided Hereditary factor XI deficiency disease
Reversed 0
HGVS NC_000004.11:g.187208954G>A
CLNSRC UniProtKB (variants)
CLNACC RCV000059018.1, RCV000169135.1,