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rs1060501878

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060501878(A;T)
Make rs1060501878(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position89773304
GeneFANCA
is asnp
is mentioned by
dbSNPrs1060501878
dbSNP (old)rs1060501878
ClinGenrs1060501878
ebirs1060501878
HLIrs1060501878
Exacrs1060501878
Gnomadrs1060501878
Varsomers1060501878
LitVarrs1060501878
Maprs1060501878
PheGenIrs1060501878
Biobankrs1060501878
1000 genomesrs1060501878
hgdprs1060501878
ensemblrs1060501878
gopubmedrs1060501878
geneviewrs1060501878
scholarrs1060501878
googlers1060501878
pharmgkbrs1060501878
gwascentralrs1060501878
openSNPrs1060501878
23andMers1060501878
23andMe allrs1060501878
SNPshotrs1060501878
SNPdbers1060501878
MSV3drs1060501878
GWAS Ctlgrs1060501878
Max Magnitude0
ClinVar
Risk rs1060501878(T;T)
Alt rs1060501878(T;T)
Reference Rs1060501878(A;A)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia
Reversed 1
HGVS NC_000016.9:g.89839712T>A
CLNSRC
CLNACC RCV000475930.1,