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rs1060501876

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501876(-;-)
Make rs1060501876(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position89767196
GeneFANCA
is asnp
is mentioned by
dbSNPrs1060501876
dbSNP (old)rs1060501876
ClinGenrs1060501876
ebirs1060501876
HLIrs1060501876
Exacrs1060501876
Gnomadrs1060501876
Varsomers1060501876
Maprs1060501876
PheGenIrs1060501876
Biobankrs1060501876
1000 genomesrs1060501876
hgdprs1060501876
ensemblrs1060501876
gopubmedrs1060501876
geneviewrs1060501876
scholarrs1060501876
googlers1060501876
pharmgkbrs1060501876
gwascentralrs1060501876
openSNPrs1060501876
23andMers1060501876
23andMe allrs1060501876
SNPshotrs1060501876
SNPdbers1060501876
MSV3drs1060501876
GWAS Ctlgrs1060501876
Max Magnitude0
ClinVar
Risk rs1060501876(-;-)
Alt rs1060501876(-;-)
Reference Rs1060501876(C;C)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia
Reversed 1
HGVS NC_000016.9:g.89833604delG
CLNSRC
CLNACC RCV000470001.1,