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rs863223975

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223975(A;C)
Make rs863223975(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241500511
GeneFH
is asnp
is mentioned by
dbSNPrs863223975
ebirs863223975
HLIrs863223975
Exacrs863223975
Varsomers863223975
Maprs863223975
PheGenIrs863223975
hapmaprs863223975
1000 genomesrs863223975
hgdprs863223975
ensemblrs863223975
gopubmedrs863223975
geneviewrs863223975
scholarrs863223975
googlers863223975
pharmgkbrs863223975
gwascentralrs863223975
openSNPrs863223975
23andMers863223975
23andMe allrs863223975
SNP Nexus

SNPshotrs863223975
SNPdbers863223975
MSV3drs863223975
GWAS Ctlgrs863223975
Max Magnitude0
ClinVar
Risk rs863223975(C;C)
Alt rs863223975(C;C)
Reference rs863223975(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241663811T>G
CLNSRC
CLNACC RCV000196513.1,