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rs863224016

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863224016(-;T)
Make rs863224016(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241504093
GeneFH
is asnp
is mentioned by
dbSNPrs863224016
ClinGenrs863224016
ebirs863224016
HLIrs863224016
Exacrs863224016
Varsomers863224016
Maprs863224016
PheGenIrs863224016
hapmaprs863224016
1000 genomesrs863224016
hgdprs863224016
ensemblrs863224016
gopubmedrs863224016
geneviewrs863224016
scholarrs863224016
googlers863224016
pharmgkbrs863224016
gwascentralrs863224016
openSNPrs863224016
23andMers863224016
23andMe allrs863224016
SNP Nexus

SNPshotrs863224016
SNPdbers863224016
MSV3drs863224016
GWAS Ctlgrs863224016
Max Magnitude0
ClinVar
Risk rs863224016(T;T)
Alt rs863224016(T;T)
Reference Rs863224016(;)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241667394dupA
CLNSRC
CLNACC RCV000197689.1,