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rs863223967

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223967(A;G)
Make rs863223967(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241508653
GeneFH
is asnp
is mentioned by
dbSNPrs863223967
ebirs863223967
HLIrs863223967
Exacrs863223967
Varsomers863223967
Maprs863223967
PheGenIrs863223967
hapmaprs863223967
1000 genomesrs863223967
hgdprs863223967
ensemblrs863223967
gopubmedrs863223967
geneviewrs863223967
scholarrs863223967
googlers863223967
pharmgkbrs863223967
gwascentralrs863223967
openSNPrs863223967
23andMers863223967
23andMe allrs863223967
SNP Nexus

SNPshotrs863223967
SNPdbers863223967
MSV3drs863223967
GWAS Ctlgrs863223967
Max Magnitude0
ClinVar
Risk rs863223967(G;G)
Alt rs863223967(G;G)
Reference rs863223967(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241671953T>C
CLNSRC
CLNACC RCV000198721.1,