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rs863224005

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224005(A;G)
Make rs863224005(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241502567
GeneFH
is asnp
is mentioned by
dbSNPrs863224005
ebirs863224005
HLIrs863224005
Exacrs863224005
Varsomers863224005
Maprs863224005
PheGenIrs863224005
hapmaprs863224005
1000 genomesrs863224005
hgdprs863224005
ensemblrs863224005
gopubmedrs863224005
geneviewrs863224005
scholarrs863224005
googlers863224005
pharmgkbrs863224005
gwascentralrs863224005
openSNPrs863224005
23andMers863224005
23andMe allrs863224005
SNP Nexus

SNPshotrs863224005
SNPdbers863224005
MSV3drs863224005
GWAS Ctlgrs863224005
Max Magnitude0
ClinVar
Risk rs863224005(G;G)
Alt rs863224005(G;G)
Reference rs863224005(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241665867T>C
CLNSRC
CLNACC RCV000197014.1,