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rs1057519366

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057519366(-;C)
Make rs1057519366(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95150013
GeneFANCC
is asnp
is mentioned by
dbSNPrs1057519366
dbSNP (old)rs1057519366
ClinGenrs1057519366
ebirs1057519366
HLIrs1057519366
Exacrs1057519366
Gnomadrs1057519366
Varsomers1057519366
Maprs1057519366
PheGenIrs1057519366
Biobankrs1057519366
1000 genomesrs1057519366
hgdprs1057519366
ensemblrs1057519366
gopubmedrs1057519366
geneviewrs1057519366
scholarrs1057519366
googlers1057519366
pharmgkbrs1057519366
gwascentralrs1057519366
openSNPrs1057519366
23andMers1057519366
23andMe allrs1057519366
SNPshotrs1057519366
SNPdbers1057519366
MSV3drs1057519366
GWAS Ctlgrs1057519366
Max Magnitude0
ClinVar
Risk rs1057519366(C;C)
Alt rs1057519366(C;C)
Reference Rs1057519366(-;-)
Significance Probable-Pathogenic
Disease Carcinoma of colon
Variation info
Gene FANCC
CLNDBN Carcinoma of colon
Reversed 1
HGVS NC_000009.11:g.97912296dupG
CLNSRC
CLNACC RCV000416810.1,