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rs1064795597

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Chromosome9
Position95117343
GeneC9orf3, FANCC
is asnp
is mentioned by
dbSNPrs1064795597
dbSNP (old)rs1064795597
ClinGenrs1064795597
ebirs1064795597
HLIrs1064795597
Exacrs1064795597
Gnomadrs1064795597
Varsomers1064795597
LitVarrs1064795597
Maprs1064795597
PheGenIrs1064795597
Biobankrs1064795597
1000 genomesrs1064795597
hgdprs1064795597
ensemblrs1064795597
gopubmedrs1064795597
geneviewrs1064795597
scholarrs1064795597
googlers1064795597
pharmgkbrs1064795597
gwascentralrs1064795597
openSNPrs1064795597
23andMers1064795597
23andMe allrs1064795597
SNPshotrs1064795597
SNPdbers1064795597
MSV3drs1064795597
GWAS Ctlgrs1064795597
Max Magnitude0
ClinVar
Risk rs1064795597(-;-)
Alt rs1064795597(-;-)
Reference Rs1064795597(TT;TT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FANCC
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.97879625_97879626delAA
CLNSRC
CLNACC RCV000482484.1,