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rs863223983

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223983(A;G)
Make rs863223983(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241512083
GeneFH
is asnp
is mentioned by
dbSNPrs863223983
ebirs863223983
HLIrs863223983
Exacrs863223983
Varsomers863223983
Maprs863223983
PheGenIrs863223983
hapmaprs863223983
1000 genomesrs863223983
hgdprs863223983
ensemblrs863223983
gopubmedrs863223983
geneviewrs863223983
scholarrs863223983
googlers863223983
pharmgkbrs863223983
gwascentralrs863223983
openSNPrs863223983
23andMers863223983
23andMe allrs863223983
SNP Nexus

SNPshotrs863223983
SNPdbers863223983
MSV3drs863223983
GWAS Ctlgrs863223983
Max Magnitude0
ClinVar
Risk rs863223983(G;G)
Alt rs863223983(G;G)
Reference rs863223983(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241675383T>C
CLNSRC
CLNACC RCV000197876.1,