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

rs863223973

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223973(G;G)
Make rs863223973(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241504127
GeneFH
is asnp
is mentioned by
dbSNPrs863223973
ebirs863223973
HLIrs863223973
Exacrs863223973
Varsomers863223973
Maprs863223973
PheGenIrs863223973
hapmaprs863223973
1000 genomesrs863223973
hgdprs863223973
ensemblrs863223973
gopubmedrs863223973
geneviewrs863223973
scholarrs863223973
googlers863223973
pharmgkbrs863223973
gwascentralrs863223973
openSNPrs863223973
23andMers863223973
23andMe allrs863223973
SNP Nexus

SNPshotrs863223973
SNPdbers863223973
MSV3drs863223973
GWAS Ctlgrs863223973
Max Magnitude0
ClinVar
Risk rs863223973(G;G)
Alt rs863223973(G;G)
Reference rs863223973(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241667427A>C
CLNSRC
CLNACC RCV000195561.1,