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

rs863224010

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224010(A;G)
Make rs863224010(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241497967
GeneFH
is asnp
is mentioned by
dbSNPrs863224010
ebirs863224010
HLIrs863224010
Exacrs863224010
Varsomers863224010
Maprs863224010
PheGenIrs863224010
hapmaprs863224010
1000 genomesrs863224010
hgdprs863224010
ensemblrs863224010
gopubmedrs863224010
geneviewrs863224010
scholarrs863224010
googlers863224010
pharmgkbrs863224010
gwascentralrs863224010
openSNPrs863224010
23andMers863224010
23andMe allrs863224010
SNP Nexus

SNPshotrs863224010
SNPdbers863224010
MSV3drs863224010
GWAS Ctlgrs863224010
Max Magnitude0
ClinVar
Risk rs863224010(G;G)
Alt rs863224010(G;G)
Reference rs863224010(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241661267T>C
CLNSRC
CLNACC RCV000197211.2,