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rs863224002

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224002(A;A)
Make rs863224002(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241504203
GeneFH
is asnp
is mentioned by
dbSNPrs863224002
ebirs863224002
HLIrs863224002
Exacrs863224002
Varsomers863224002
Maprs863224002
PheGenIrs863224002
hapmaprs863224002
1000 genomesrs863224002
hgdprs863224002
ensemblrs863224002
gopubmedrs863224002
geneviewrs863224002
scholarrs863224002
googlers863224002
pharmgkbrs863224002
gwascentralrs863224002
openSNPrs863224002
23andMers863224002
23andMe allrs863224002
SNP Nexus

SNPshotrs863224002
SNPdbers863224002
MSV3drs863224002
GWAS Ctlgrs863224002
Max Magnitude0
ClinVar
Risk rs863224002(A;A)
Alt rs863224002(A;A)
Reference rs863224002(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241667503G>T
CLNSRC
CLNACC RCV000199702.2,