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rs863223981

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223981(-;T)
Make rs863223981(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241506109
GeneFH
is asnp
is mentioned by
dbSNPrs863223981
dbSNP (old)rs863223981
ClinGenrs863223981
ebirs863223981
HLIrs863223981
Exacrs863223981
Varsomers863223981
Maprs863223981
PheGenIrs863223981
Biobankrs863223981
1000 genomesrs863223981
hgdprs863223981
ensemblrs863223981
gopubmedrs863223981
geneviewrs863223981
scholarrs863223981
googlers863223981
pharmgkbrs863223981
gwascentralrs863223981
openSNPrs863223981
23andMers863223981
23andMe allrs863223981
SNP Nexus

SNPshotrs863223981
SNPdbers863223981
MSV3drs863223981
GWAS Ctlgrs863223981
Max Magnitude0
ClinVar
Risk rs863223981(T;T)
Alt rs863223981(T;T)
Reference Rs863223981(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241669410dupA
CLNSRC
CLNACC RCV000195789.1,