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rs121918192

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918192(C;G)
Make rs121918192(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position94603547
GeneFBP1
is asnp
is mentioned by
dbSNPrs121918192
ebirs121918192
HLIrs121918192
Exacrs121918192
Varsomers121918192
Maprs121918192
PheGenIrs121918192
hapmaprs121918192
1000 genomesrs121918192
hgdprs121918192
ensemblrs121918192
gopubmedrs121918192
geneviewrs121918192
scholarrs121918192
googlers121918192
pharmgkbrs121918192
gwascentralrs121918192
openSNPrs121918192
23andMers121918192
23andMe allrs121918192
SNP Nexus

SNPshotrs121918192
SNPdbers121918192
MSV3drs121918192
GWAS Ctlgrs121918192
Max Magnitude0
OMIM611570
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121918192(G;G)
Alt rs121918192(G;G)
Reference rs121918192(C;C)
Significance Pathogenic
Disease Fructose-biphosphatase deficiency
Variation info
Gene FBP1
CLNDBN Fructose-biphosphatase deficiency
Reversed 1
HGVS NC_000009.11:g.97365829G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000000920.4,