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rs121434505

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434505(C;T)
Make rs121434505(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position35455853
GeneFANCE
is asnp
is mentioned by
dbSNPrs121434505
ebirs121434505
HLIrs121434505
Exacrs121434505
Varsomers121434505
Maprs121434505
PheGenIrs121434505
hapmaprs121434505
1000 genomesrs121434505
hgdprs121434505
ensemblrs121434505
gopubmedrs121434505
geneviewrs121434505
scholarrs121434505
googlers121434505
pharmgkbrs121434505
gwascentralrs121434505
openSNPrs121434505
23andMers121434505
23andMe allrs121434505
SNP Nexus

SNPshotrs121434505
SNPdbers121434505
MSV3drs121434505
GWAS Ctlgrs121434505
Max Magnitude0
OMIM600901
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434505(T;T)
Alt rs121434505(T;T)
Reference rs121434505(C;C)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCE
CLNDBN Fanconi anemia, complementation group E
Reversed 0
HGVS NC_000006.11:g.35423630C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009247.2,