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rs1060501880

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501880(C;T)
Make rs1060501880(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position89764919
GeneFANCA
is asnp
is mentioned by
dbSNPrs1060501880
dbSNP (old)rs1060501880
ClinGenrs1060501880
ebirs1060501880
HLIrs1060501880
Exacrs1060501880
Gnomadrs1060501880
Varsomers1060501880
LitVarrs1060501880
Maprs1060501880
PheGenIrs1060501880
Biobankrs1060501880
1000 genomesrs1060501880
hgdprs1060501880
ensemblrs1060501880
gopubmedrs1060501880
geneviewrs1060501880
scholarrs1060501880
googlers1060501880
pharmgkbrs1060501880
gwascentralrs1060501880
openSNPrs1060501880
23andMers1060501880
23andMe allrs1060501880
SNPshotrs1060501880
SNPdbers1060501880
MSV3drs1060501880
GWAS Ctlgrs1060501880
Max Magnitude0
ClinVar
Risk rs1060501880(T;T)
Alt rs1060501880(T;T)
Reference Rs1060501880(C;C)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia
Reversed 1
HGVS NC_000016.9:g.89831327G>A
CLNSRC
CLNACC RCV000465485.1,