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

rs863223970

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223970(A;A)
Make rs863223970(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241506029
GeneFH
is asnp
is mentioned by
dbSNPrs863223970
ebirs863223970
HLIrs863223970
Exacrs863223970
Varsomers863223970
Maprs863223970
PheGenIrs863223970
hapmaprs863223970
1000 genomesrs863223970
hgdprs863223970
ensemblrs863223970
gopubmedrs863223970
geneviewrs863223970
scholarrs863223970
googlers863223970
pharmgkbrs863223970
gwascentralrs863223970
openSNPrs863223970
23andMers863223970
23andMe allrs863223970
SNP Nexus

SNPshotrs863223970
SNPdbers863223970
MSV3drs863223970
GWAS Ctlgrs863223970
Max Magnitude0
ClinVar
Risk rs863223970(A;A)
Alt rs863223970(A;A)
Reference rs863223970(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241669329A>T
CLNSRC
CLNACC RCV000198919.1,