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rs878854342

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854342(A;A)
Make rs878854342(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position35459323
GeneFANCE
is asnp
is mentioned by
dbSNPrs878854342
ebirs878854342
HLIrs878854342
Exacrs878854342
Varsomers878854342
Maprs878854342
PheGenIrs878854342
hapmaprs878854342
1000 genomesrs878854342
hgdprs878854342
ensemblrs878854342
gopubmedrs878854342
geneviewrs878854342
scholarrs878854342
googlers878854342
pharmgkbrs878854342
gwascentralrs878854342
openSNPrs878854342
23andMers878854342
23andMe allrs878854342
SNP Nexus

SNPshotrs878854342
SNPdbers878854342
MSV3drs878854342
GWAS Ctlgrs878854342
Max Magnitude0
ClinVar
Risk rs878854342(A;A)
Alt rs878854342(A;A)
Reference rs878854342(G;G)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCE
CLNDBN Fanconi anemia, complementation group E
Reversed 0
HGVS NC_000006.11:g.35427100G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009249.3,