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rs863223965

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223965(C;C)
Make rs863223965(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241508757
GeneFH
is asnp
is mentioned by
dbSNPrs863223965
ebirs863223965
HLIrs863223965
Exacrs863223965
Varsomers863223965
Maprs863223965
PheGenIrs863223965
hapmaprs863223965
1000 genomesrs863223965
hgdprs863223965
ensemblrs863223965
gopubmedrs863223965
geneviewrs863223965
scholarrs863223965
googlers863223965
pharmgkbrs863223965
gwascentralrs863223965
openSNPrs863223965
23andMers863223965
23andMe allrs863223965
SNP Nexus

SNPshotrs863223965
SNPdbers863223965
MSV3drs863223965
GWAS Ctlgrs863223965
Max Magnitude0
ClinVar
Risk rs863223965(C;C)
Alt rs863223965(C;C)
Reference rs863223965(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241672057A>G
CLNSRC
CLNACC RCV000200358.1,