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rs863223972

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223972(G;G)
Make rs863223972(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241504143
GeneFH
is asnp
is mentioned by
dbSNPrs863223972
ebirs863223972
HLIrs863223972
Exacrs863223972
Varsomers863223972
Maprs863223972
PheGenIrs863223972
hapmaprs863223972
1000 genomesrs863223972
hgdprs863223972
ensemblrs863223972
gopubmedrs863223972
geneviewrs863223972
scholarrs863223972
googlers863223972
pharmgkbrs863223972
gwascentralrs863223972
openSNPrs863223972
23andMers863223972
23andMe allrs863223972
SNP Nexus

SNPshotrs863223972
SNPdbers863223972
MSV3drs863223972
GWAS Ctlgrs863223972
Max Magnitude0
ClinVar
Risk rs863223972(G;G)
Alt rs863223972(G;G)
Reference rs863223972(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241667443A>C
CLNSRC
CLNACC RCV000197952.1,