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rs863224004

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224004(A;A)
Make rs863224004(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241504053
GeneFH
is asnp
is mentioned by
dbSNPrs863224004
ebirs863224004
HLIrs863224004
Exacrs863224004
Varsomers863224004
Maprs863224004
PheGenIrs863224004
hapmaprs863224004
1000 genomesrs863224004
hgdprs863224004
ensemblrs863224004
gopubmedrs863224004
geneviewrs863224004
scholarrs863224004
googlers863224004
pharmgkbrs863224004
gwascentralrs863224004
openSNPrs863224004
23andMers863224004
23andMe allrs863224004
SNP Nexus

SNPshotrs863224004
SNPdbers863224004
MSV3drs863224004
GWAS Ctlgrs863224004
Max Magnitude0
ClinVar
Risk rs863224004(A;A)
Alt rs863224004(A;A)
Reference rs863224004(G;G)
Significance Pathogenic
Disease not provided Fumarase deficiency
Variation info
Gene FH
CLNDBN not provided Fumarase deficiency
Reversed 1
HGVS NC_000001.10:g.241667353C>T
CLNSRC
CLNACC RCV000200592.2, RCV000234564.1,