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rs863224014

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224014(A;T)
Make rs863224014(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241512058
GeneFH
is asnp
is mentioned by
dbSNPrs863224014
ebirs863224014
HLIrs863224014
Exacrs863224014
Varsomers863224014
Maprs863224014
PheGenIrs863224014
hapmaprs863224014
1000 genomesrs863224014
hgdprs863224014
ensemblrs863224014
gopubmedrs863224014
geneviewrs863224014
scholarrs863224014
googlers863224014
pharmgkbrs863224014
gwascentralrs863224014
openSNPrs863224014
23andMers863224014
23andMe allrs863224014
SNP Nexus

SNPshotrs863224014
SNPdbers863224014
MSV3drs863224014
GWAS Ctlgrs863224014
Max Magnitude0
ClinVar
Risk rs863224014(T;T)
Alt rs863224014(T;T)
Reference rs863224014(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241675358T>A
CLNSRC
CLNACC RCV000197488.1,