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rs863223993

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223993(-;A)
Make rs863223993(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241497960
GeneFH
is asnp
is mentioned by
dbSNPrs863223993
dbSNP (old)rs863223993
ClinGenrs863223993
ebirs863223993
HLIrs863223993
Exacrs863223993
Gnomadrs863223993
Varsomers863223993
Maprs863223993
PheGenIrs863223993
Biobankrs863223993
1000 genomesrs863223993
hgdprs863223993
ensemblrs863223993
gopubmedrs863223993
geneviewrs863223993
scholarrs863223993
googlers863223993
pharmgkbrs863223993
gwascentralrs863223993
openSNPrs863223993
23andMers863223993
23andMe allrs863223993
SNP Nexus

SNPshotrs863223993
SNPdbers863223993
MSV3drs863223993
GWAS Ctlgrs863223993
Max Magnitude0
ClinVar
Risk rs863223993(A;A)
Alt rs863223993(A;A)
Reference Rs863223993(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241661261dupT
CLNSRC
CLNACC RCV000200182.1,