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rs878853660

From SNPedia

Orientationminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs878853660(-;-)
Make rs878853660(-;GT)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position89792479
GeneFANCA
is asnp
is mentioned by
dbSNPrs878853660
ebirs878853660
HLIrs878853660
Exacrs878853660
Varsomers878853660
Maprs878853660
PheGenIrs878853660
hapmaprs878853660
1000 genomesrs878853660
hgdprs878853660
ensemblrs878853660
gopubmedrs878853660
geneviewrs878853660
scholarrs878853660
googlers878853660
pharmgkbrs878853660
gwascentralrs878853660
openSNPrs878853660
23andMers878853660
23andMe allrs878853660
SNP Nexus

SNPshotrs878853660
SNPdbers878853660
MSV3drs878853660
GWAS Ctlgrs878853660
Max Magnitude0
ClinVar
Risk rs878853660(;)
Alt rs878853660(;)
Reference rs878853660(GT;GT)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia
Reversed 1
HGVS NC_000016.9:g.89858887_89858888delAC
CLNSRC
CLNACC RCV000228729.1,