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rs863223998

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223998(C;T)
Make rs863223998(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241508605
GeneFH
is asnp
is mentioned by
dbSNPrs863223998
ebirs863223998
HLIrs863223998
Exacrs863223998
Varsomers863223998
Maprs863223998
PheGenIrs863223998
hapmaprs863223998
1000 genomesrs863223998
hgdprs863223998
ensemblrs863223998
gopubmedrs863223998
geneviewrs863223998
scholarrs863223998
googlers863223998
pharmgkbrs863223998
gwascentralrs863223998
openSNPrs863223998
23andMers863223998
23andMe allrs863223998
SNP Nexus

SNPshotrs863223998
SNPdbers863223998
MSV3drs863223998
GWAS Ctlgrs863223998
Max Magnitude0
ClinVar
Risk rs863223998(T;T)
Alt rs863223998(T;T)
Reference rs863223998(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241671905G>A
CLNSRC
CLNACC RCV000200102.2,