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rs1060501879

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501879(A;A)
Make rs1060501879(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position89791458
GeneFANCA
is asnp
is mentioned by
dbSNPrs1060501879
dbSNP (old)rs1060501879
ClinGenrs1060501879
ebirs1060501879
HLIrs1060501879
Exacrs1060501879
Gnomadrs1060501879
Varsomers1060501879
LitVarrs1060501879
Maprs1060501879
PheGenIrs1060501879
Biobankrs1060501879
1000 genomesrs1060501879
hgdprs1060501879
ensemblrs1060501879
gopubmedrs1060501879
geneviewrs1060501879
scholarrs1060501879
googlers1060501879
pharmgkbrs1060501879
gwascentralrs1060501879
openSNPrs1060501879
23andMers1060501879
23andMe allrs1060501879
SNPshotrs1060501879
SNPdbers1060501879
MSV3drs1060501879
GWAS Ctlgrs1060501879
Max Magnitude0
ClinVar
Risk rs1060501879(A;A)
Alt rs1060501879(A;A)
Reference Rs1060501879(G;G)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia
Reversed 1
HGVS NC_000016.9:g.89857866C>T
CLNSRC
CLNACC RCV000464366.1,