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rs863224015

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224015(A;G)
Make rs863224015(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241511983
GeneFH
is asnp
is mentioned by
dbSNPrs863224015
ebirs863224015
HLIrs863224015
Exacrs863224015
Varsomers863224015
Maprs863224015
PheGenIrs863224015
hapmaprs863224015
1000 genomesrs863224015
hgdprs863224015
ensemblrs863224015
gopubmedrs863224015
geneviewrs863224015
scholarrs863224015
googlers863224015
pharmgkbrs863224015
gwascentralrs863224015
openSNPrs863224015
23andMers863224015
23andMe allrs863224015
SNP Nexus

SNPshotrs863224015
SNPdbers863224015
MSV3drs863224015
GWAS Ctlgrs863224015
Max Magnitude0
ClinVar
Risk rs863224015(G;G)
Alt rs863224015(G;G)
Reference rs863224015(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241675283T>C
CLNSRC
CLNACC RCV000200019.1,