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rs863223976

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223976(G;T)
Make rs863223976(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241500500
GeneFH
is asnp
is mentioned by
dbSNPrs863223976
ebirs863223976
HLIrs863223976
Exacrs863223976
Varsomers863223976
Maprs863223976
PheGenIrs863223976
hapmaprs863223976
1000 genomesrs863223976
hgdprs863223976
ensemblrs863223976
gopubmedrs863223976
geneviewrs863223976
scholarrs863223976
googlers863223976
pharmgkbrs863223976
gwascentralrs863223976
openSNPrs863223976
23andMers863223976
23andMe allrs863223976
SNP Nexus

SNPshotrs863223976
SNPdbers863223976
MSV3drs863223976
GWAS Ctlgrs863223976
Max Magnitude0
ClinVar
Risk rs863223976(T;T)
Alt rs863223976(T;T)
Reference rs863223976(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241663800C>A
CLNSRC
CLNACC RCV000198349.1,