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rs1057516919

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs1057516919(-;-)
Make rs1057516919(-;TG)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95114679
GeneC9orf3, FANCC
is asnp
is mentioned by
dbSNPrs1057516919
dbSNP (old)rs1057516919
ClinGenrs1057516919
ebirs1057516919
HLIrs1057516919
Exacrs1057516919
Gnomadrs1057516919
Varsomers1057516919
Maprs1057516919
PheGenIrs1057516919
Biobankrs1057516919
1000 genomesrs1057516919
hgdprs1057516919
ensemblrs1057516919
gopubmedrs1057516919
geneviewrs1057516919
scholarrs1057516919
googlers1057516919
pharmgkbrs1057516919
gwascentralrs1057516919
openSNPrs1057516919
23andMers1057516919
23andMe allrs1057516919
SNPshotrs1057516919
SNPdbers1057516919
MSV3drs1057516919
GWAS Ctlgrs1057516919
Max Magnitude0
ClinVar
Risk rs1057516919(-;-)
Alt rs1057516919(-;-)
Reference Rs1057516919(TG;TG)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C
Reversed 1
HGVS NC_000009.11:g.97876961_97876962delCA
CLNSRC
CLNACC RCV000410408.1,