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rs878853671

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853671(-;-)
Make rs878853671(-;G)
Make rs878853671(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position95249262
GeneFANCC
is asnp
is mentioned by
dbSNPrs878853671
ebirs878853671
HLIrs878853671
Exacrs878853671
Varsomers878853671
Maprs878853671
PheGenIrs878853671
hapmaprs878853671
1000 genomesrs878853671
hgdprs878853671
ensemblrs878853671
gopubmedrs878853671
geneviewrs878853671
scholarrs878853671
googlers878853671
pharmgkbrs878853671
gwascentralrs878853671
openSNPrs878853671
23andMers878853671
23andMe allrs878853671
SNP Nexus

SNPshotrs878853671
SNPdbers878853671
MSV3drs878853671
GWAS Ctlgrs878853671
Max Magnitude0
ClinVar
Risk rs878853671(G;G)
Alt rs878853671(G;G)
Reference rs878853671(;)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia
Reversed 1
HGVS NC_000009.11:g.98011545dupC
CLNSRC
CLNACC RCV000226528.1,