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rs863223974

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223974(A;T)
Make rs863223974(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241502511
GeneFH
is asnp
is mentioned by
dbSNPrs863223974
ebirs863223974
HLIrs863223974
Exacrs863223974
Varsomers863223974
Maprs863223974
PheGenIrs863223974
hapmaprs863223974
1000 genomesrs863223974
hgdprs863223974
ensemblrs863223974
gopubmedrs863223974
geneviewrs863223974
scholarrs863223974
googlers863223974
pharmgkbrs863223974
gwascentralrs863223974
openSNPrs863223974
23andMers863223974
23andMe allrs863223974
SNP Nexus

SNPshotrs863223974
SNPdbers863223974
MSV3drs863223974
GWAS Ctlgrs863223974
Max Magnitude0
ClinVar
Risk rs863223974(T;T)
Alt rs863223974(T;T)
Reference rs863223974(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241665811T>A
CLNSRC
CLNACC RCV000197462.2,