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rs863223987

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GCC;GCC) 0 common in clinvar
Make rs863223987(ACT;ACT)
Make rs863223987(ACT;GCC)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241504044
GeneFH
is asnp
is mentioned by
dbSNPrs863223987
ClinGenrs863223987
ebirs863223987
HLIrs863223987
Exacrs863223987
Varsomers863223987
Maprs863223987
PheGenIrs863223987
hapmaprs863223987
1000 genomesrs863223987
hgdprs863223987
ensemblrs863223987
gopubmedrs863223987
geneviewrs863223987
scholarrs863223987
googlers863223987
pharmgkbrs863223987
gwascentralrs863223987
openSNPrs863223987
23andMers863223987
23andMe allrs863223987
SNP Nexus

SNPshotrs863223987
SNPdbers863223987
MSV3drs863223987
GWAS Ctlgrs863223987
Max Magnitude0
ClinVar
Risk rs863223987(ACT;ACT)
Alt rs863223987(ACT;ACT)
Reference Rs863223987(GCC;GCC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241667344_241667346delGGCinsAGT
CLNSRC
CLNACC RCV000198761.2,