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rs863223969

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223969(A;A)
Make rs863223969(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241506068
GeneFH
is asnp
is mentioned by
dbSNPrs863223969
ebirs863223969
HLIrs863223969
Exacrs863223969
Varsomers863223969
Maprs863223969
PheGenIrs863223969
hapmaprs863223969
1000 genomesrs863223969
hgdprs863223969
ensemblrs863223969
gopubmedrs863223969
geneviewrs863223969
scholarrs863223969
googlers863223969
pharmgkbrs863223969
gwascentralrs863223969
openSNPrs863223969
23andMers863223969
23andMe allrs863223969
SNP Nexus

SNPshotrs863223969
SNPdbers863223969
MSV3drs863223969
GWAS Ctlgrs863223969
Max Magnitude0
ClinVar
Risk rs863223969(A;A)
Alt rs863223969(A;A)
Reference rs863223969(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene FH
CLNDBN not specified
Reversed 1
HGVS NC_000001.10:g.241669368C>T
CLNSRC
CLNACC RCV000197030.2,