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

rs863224008

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224008(A;T)
Make rs863224008(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241497972
GeneFH
is asnp
is mentioned by
dbSNPrs863224008
ebirs863224008
HLIrs863224008
Exacrs863224008
Varsomers863224008
Maprs863224008
PheGenIrs863224008
hapmaprs863224008
1000 genomesrs863224008
hgdprs863224008
ensemblrs863224008
gopubmedrs863224008
geneviewrs863224008
scholarrs863224008
googlers863224008
pharmgkbrs863224008
gwascentralrs863224008
openSNPrs863224008
23andMers863224008
23andMe allrs863224008
SNP Nexus

SNPshotrs863224008
SNPdbers863224008
MSV3drs863224008
GWAS Ctlgrs863224008
Max Magnitude0
ClinVar
Risk rs863224008(T;T)
Alt rs863224008(T;T)
Reference rs863224008(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241661272T>A
CLNSRC
CLNACC RCV000198930.1,