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rs863223979

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223979(A;C)
Make rs863223979(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241497915
GeneFH
is asnp
is mentioned by
dbSNPrs863223979
ebirs863223979
HLIrs863223979
Exacrs863223979
Varsomers863223979
Maprs863223979
PheGenIrs863223979
hapmaprs863223979
1000 genomesrs863223979
hgdprs863223979
ensemblrs863223979
gopubmedrs863223979
geneviewrs863223979
scholarrs863223979
googlers863223979
pharmgkbrs863223979
gwascentralrs863223979
openSNPrs863223979
23andMers863223979
23andMe allrs863223979
SNP Nexus

SNPshotrs863223979
SNPdbers863223979
MSV3drs863223979
GWAS Ctlgrs863223979
Max Magnitude0
ClinVar
Risk rs863223979(C;C)
Alt rs863223979(C;C)
Reference rs863223979(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241661215T>G
CLNSRC
CLNACC RCV000198419.1,