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rs863224011

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224011(A;A)
Make rs863224011(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241517317
GeneFH
is asnp
is mentioned by
dbSNPrs863224011
ebirs863224011
HLIrs863224011
Exacrs863224011
Varsomers863224011
Maprs863224011
PheGenIrs863224011
hapmaprs863224011
1000 genomesrs863224011
hgdprs863224011
ensemblrs863224011
gopubmedrs863224011
geneviewrs863224011
scholarrs863224011
googlers863224011
pharmgkbrs863224011
gwascentralrs863224011
openSNPrs863224011
23andMers863224011
23andMe allrs863224011
SNP Nexus

SNPshotrs863224011
SNPdbers863224011
MSV3drs863224011
GWAS Ctlgrs863224011
Max Magnitude0
ClinVar
Risk rs863224011(A;A)
Alt rs863224011(A;A)
Reference rs863224011(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241680617C>T
CLNSRC
CLNACC RCV000199125.1,