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rs863223997

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223997(C;T)
Make rs863223997(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241508632
GeneFH
is asnp
is mentioned by
dbSNPrs863223997
ebirs863223997
HLIrs863223997
Exacrs863223997
Varsomers863223997
Maprs863223997
PheGenIrs863223997
hapmaprs863223997
1000 genomesrs863223997
hgdprs863223997
ensemblrs863223997
gopubmedrs863223997
geneviewrs863223997
scholarrs863223997
googlers863223997
pharmgkbrs863223997
gwascentralrs863223997
openSNPrs863223997
23andMers863223997
23andMe allrs863223997
SNP Nexus

SNPshotrs863223997
SNPdbers863223997
MSV3drs863223997
GWAS Ctlgrs863223997
Max Magnitude0
ClinVar
Risk rs863223997(T;T)
Alt rs863223997(T;T)
Reference rs863223997(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241671932G>A
CLNSRC
CLNACC RCV000197574.1,