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rs863224009

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224009(G;G)
Make rs863224009(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241500559
GeneFH
is asnp
is mentioned by
dbSNPrs863224009
ebirs863224009
HLIrs863224009
Exacrs863224009
Varsomers863224009
Maprs863224009
PheGenIrs863224009
hapmaprs863224009
1000 genomesrs863224009
hgdprs863224009
ensemblrs863224009
gopubmedrs863224009
geneviewrs863224009
scholarrs863224009
googlers863224009
pharmgkbrs863224009
gwascentralrs863224009
openSNPrs863224009
23andMers863224009
23andMe allrs863224009
SNP Nexus

SNPshotrs863224009
SNPdbers863224009
MSV3drs863224009
GWAS Ctlgrs863224009
Max Magnitude0
ClinVar
Risk rs863224009(G;G)
Alt rs863224009(G;G)
Reference rs863224009(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241663859A>C
CLNSRC
CLNACC RCV000196004.2,