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rs1060499606

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTCAT;CTCAT) 0 common in clinvar
Make rs1060499606(-;-)
Make rs1060499606(-;CTCAT)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95172133
GeneFANCC
is asnp
is mentioned by
dbSNPrs1060499606
dbSNP (old)rs1060499606
ClinGenrs1060499606
ebirs1060499606
HLIrs1060499606
Exacrs1060499606
Gnomadrs1060499606
Varsomers1060499606
Maprs1060499606
PheGenIrs1060499606
Biobankrs1060499606
1000 genomesrs1060499606
hgdprs1060499606
ensemblrs1060499606
gopubmedrs1060499606
geneviewrs1060499606
scholarrs1060499606
googlers1060499606
pharmgkbrs1060499606
gwascentralrs1060499606
openSNPrs1060499606
23andMers1060499606
23andMe allrs1060499606
SNPshotrs1060499606
SNPdbers1060499606
MSV3drs1060499606
GWAS Ctlgrs1060499606
Max Magnitude0
ClinVar
Risk rs1060499606(-;-)
Alt rs1060499606(-;-)
Reference Rs1060499606(CTCAT;CTCAT)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C
Reversed 1
HGVS NC_000009.11:g.97934415_97934419delATGAG
CLNSRC
CLNACC RCV000477851.1,