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rs878853663

From SNPedia

Orientationminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs878853663(-;-)
Make rs878853663(-;CT)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position89764937
GeneFANCA
is asnp
is mentioned by
dbSNPrs878853663
ebirs878853663
HLIrs878853663
Exacrs878853663
Varsomers878853663
Maprs878853663
PheGenIrs878853663
hapmaprs878853663
1000 genomesrs878853663
hgdprs878853663
ensemblrs878853663
gopubmedrs878853663
geneviewrs878853663
scholarrs878853663
googlers878853663
pharmgkbrs878853663
gwascentralrs878853663
openSNPrs878853663
23andMers878853663
23andMe allrs878853663
SNP Nexus

SNPshotrs878853663
SNPdbers878853663
MSV3drs878853663
GWAS Ctlgrs878853663
Max Magnitude0
ClinVar
Risk rs878853663(;)
Alt rs878853663(;)
Reference rs878853663(CT;CT)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia
Reversed 1
HGVS NC_000016.9:g.89831345_89831346delAG
CLNSRC
CLNACC RCV000231136.1,