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rs863224003

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224003(G;G)
Make rs863224003(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241504185
GeneFH
is asnp
is mentioned by
dbSNPrs863224003
ebirs863224003
HLIrs863224003
Exacrs863224003
Varsomers863224003
Maprs863224003
PheGenIrs863224003
hapmaprs863224003
1000 genomesrs863224003
hgdprs863224003
ensemblrs863224003
gopubmedrs863224003
geneviewrs863224003
scholarrs863224003
googlers863224003
pharmgkbrs863224003
gwascentralrs863224003
openSNPrs863224003
23andMers863224003
23andMe allrs863224003
SNP Nexus

SNPshotrs863224003
SNPdbers863224003
MSV3drs863224003
GWAS Ctlgrs863224003
Max Magnitude0
ClinVar
Risk rs863224003(G;G)
Alt rs863224003(G;G)
Reference rs863224003(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241667485A>C
CLNSRC
CLNACC RCV000196089.2,