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rs863223999

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223999(A;A)
Make rs863223999(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241506002
GeneFH
is asnp
is mentioned by
dbSNPrs863223999
ebirs863223999
HLIrs863223999
Exacrs863223999
Varsomers863223999
Maprs863223999
PheGenIrs863223999
hapmaprs863223999
1000 genomesrs863223999
hgdprs863223999
ensemblrs863223999
gopubmedrs863223999
geneviewrs863223999
scholarrs863223999
googlers863223999
pharmgkbrs863223999
gwascentralrs863223999
openSNPrs863223999
23andMers863223999
23andMe allrs863223999
SNP Nexus

SNPshotrs863223999
SNPdbers863223999
MSV3drs863223999
GWAS Ctlgrs863223999
Max Magnitude0
ClinVar
Risk rs863223999(A;A)
Alt rs863223999(A;A)
Reference rs863223999(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241669302C>T
CLNSRC
CLNACC RCV000195849.1,