Have questions? Visit https://www.reddit.com/r/SNPedia

rs863224006

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224006(A;A)
Make rs863224006(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241502533
GeneFH
is asnp
is mentioned by
dbSNPrs863224006
ebirs863224006
HLIrs863224006
Exacrs863224006
Varsomers863224006
Maprs863224006
PheGenIrs863224006
hapmaprs863224006
1000 genomesrs863224006
hgdprs863224006
ensemblrs863224006
gopubmedrs863224006
geneviewrs863224006
scholarrs863224006
googlers863224006
pharmgkbrs863224006
gwascentralrs863224006
openSNPrs863224006
23andMers863224006
23andMe allrs863224006
SNP Nexus

SNPshotrs863224006
SNPdbers863224006
MSV3drs863224006
GWAS Ctlgrs863224006
Max Magnitude0
ClinVar
Risk rs863224006(A;A)
Alt rs863224006(A;A)
Reference rs863224006(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241665833C>T
CLNSRC
CLNACC RCV000198172.1,