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rs1057516298

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057516298(C;T)
Make rs1057516298(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95107266
GeneC9orf3, FANCC, LOC107987102
is asnp
is mentioned by
dbSNPrs1057516298
dbSNP (classic)rs1057516298
ClinGenrs1057516298
ebirs1057516298
HLIrs1057516298
Exacrs1057516298
Gnomadrs1057516298
Varsomers1057516298
LitVarrs1057516298
Maprs1057516298
PheGenIrs1057516298
Biobankrs1057516298
1000 genomesrs1057516298
hgdprs1057516298
ensemblrs1057516298
geneviewrs1057516298
scholarrs1057516298
googlers1057516298
pharmgkbrs1057516298
gwascentralrs1057516298
openSNPrs1057516298
23andMers1057516298
23andMe allrs1057516298
SNPshotrs1057516298
SNPdbers1057516298
MSV3drs1057516298
GWAS Ctlgrs1057516298
Max Magnitude0
ClinVar
Risk rs1057516298(T;T)
Alt rs1057516298(T;T)
Reference Rs1057516298(C;C)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C
Reversed 1
HGVS NC_000009.11:g.97869548G>A
CLNSRC
CLNACC RCV000409733.1,