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rs863224001

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224001(A;A)
Make rs863224001(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241504213
GeneFH
is asnp
is mentioned by
dbSNPrs863224001
ebirs863224001
HLIrs863224001
Exacrs863224001
Varsomers863224001
Maprs863224001
PheGenIrs863224001
hapmaprs863224001
1000 genomesrs863224001
hgdprs863224001
ensemblrs863224001
gopubmedrs863224001
geneviewrs863224001
scholarrs863224001
googlers863224001
pharmgkbrs863224001
gwascentralrs863224001
openSNPrs863224001
23andMers863224001
23andMe allrs863224001
SNP Nexus

SNPshotrs863224001
SNPdbers863224001
MSV3drs863224001
GWAS Ctlgrs863224001
Max Magnitude0
ClinVar
Risk rs863224001(A,T;A,T)
Alt rs863224001(A,T;A,T)
Reference rs863224001(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241667513C>A; NC_000001.10:g.241667513C>T
CLNSRC
CLNACC RCV000196740.2, RCV000199631.1,