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rs863223982

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223982(A;A)
Make rs863223982(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241519591
GeneFH
is asnp
is mentioned by
dbSNPrs863223982
ebirs863223982
HLIrs863223982
Exacrs863223982
Varsomers863223982
Maprs863223982
PheGenIrs863223982
hapmaprs863223982
1000 genomesrs863223982
hgdprs863223982
ensemblrs863223982
gopubmedrs863223982
geneviewrs863223982
scholarrs863223982
googlers863223982
pharmgkbrs863223982
gwascentralrs863223982
openSNPrs863223982
23andMers863223982
23andMe allrs863223982
SNP Nexus

SNPshotrs863223982
SNPdbers863223982
MSV3drs863223982
GWAS Ctlgrs863223982
Max Magnitude0
ClinVar
Risk rs863223982(A;A)
Alt rs863223982(A;A)
Reference rs863223982(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241682891C>T
CLNSRC
CLNACC RCV000198836.1,