Have questions? Visit https://www.reddit.com/r/SNPedia

rs121964845

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964845(C;C)
Make rs121964845(C;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position6869174
GeneTPI1
is asnp
is mentioned by
dbSNPrs121964845
ebirs121964845
HLIrs121964845
Exacrs121964845
Varsomers121964845
Maprs121964845
PheGenIrs121964845
hapmaprs121964845
1000 genomesrs121964845
hgdprs121964845
ensemblrs121964845
gopubmedrs121964845
geneviewrs121964845
scholarrs121964845
googlers121964845
pharmgkbrs121964845
gwascentralrs121964845
openSNPrs121964845
23andMers121964845
23andMe allrs121964845
SNP Nexus

SNPshotrs121964845
SNPdbers121964845
MSV3drs121964845
GWAS Ctlgrs121964845
Max Magnitude0
OMIM190450
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121964845(C;C)
Alt rs121964845(C;C)
Reference rs121964845(G;G)
Significance Pathogenic
Disease Triosephosphate isomerase deficiency
Variation info
Gene TPI1
CLNDBN Triosephosphate isomerase deficiency
Reversed 0
HGVS NC_000012.11:g.6978338G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013284.26,