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rs1057517170

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517170(C;C)
Make rs1057517170(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95107064
GeneC9orf3, FANCC, LOC107987102
is asnp
is mentioned by
dbSNPrs1057517170
dbSNP (old)rs1057517170
ClinGenrs1057517170
ebirs1057517170
HLIrs1057517170
Exacrs1057517170
Gnomadrs1057517170
Varsomers1057517170
Maprs1057517170
PheGenIrs1057517170
Biobankrs1057517170
1000 genomesrs1057517170
hgdprs1057517170
ensemblrs1057517170
gopubmedrs1057517170
geneviewrs1057517170
scholarrs1057517170
googlers1057517170
pharmgkbrs1057517170
gwascentralrs1057517170
openSNPrs1057517170
23andMers1057517170
23andMe allrs1057517170
SNPshotrs1057517170
SNPdbers1057517170
MSV3drs1057517170
GWAS Ctlgrs1057517170
Max Magnitude0
ClinVar
Risk rs1057517170(C;C)
Alt rs1057517170(C;C)
Reference Rs1057517170(T;T)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C
Reversed 1
HGVS NC_000009.11:g.97869346A>G
CLNSRC
CLNACC RCV000410650.1,