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rs1064796074

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome9
Position95150014
GeneFANCC
is asnp
is mentioned by
dbSNPrs1064796074
dbSNP (old)rs1064796074
ClinGenrs1064796074
ebirs1064796074
HLIrs1064796074
Exacrs1064796074
Gnomadrs1064796074
Varsomers1064796074
Maprs1064796074
PheGenIrs1064796074
Biobankrs1064796074
1000 genomesrs1064796074
hgdprs1064796074
ensemblrs1064796074
gopubmedrs1064796074
geneviewrs1064796074
scholarrs1064796074
googlers1064796074
pharmgkbrs1064796074
gwascentralrs1064796074
openSNPrs1064796074
23andMers1064796074
23andMe allrs1064796074
SNPshotrs1064796074
SNPdbers1064796074
MSV3drs1064796074
GWAS Ctlgrs1064796074
Max Magnitude0
ClinVar
Risk rs1064796074(-;-)
Alt rs1064796074(-;-)
Reference Rs1064796074(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FANCC
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.97912296delG
CLNSRC
CLNACC RCV000483255.1,