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rs1057516792

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057516792(-;-)
Make rs1057516792(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95135358
GeneC9orf3, FANCC
is asnp
is mentioned by
dbSNPrs1057516792
dbSNP (old)rs1057516792
ClinGenrs1057516792
ebirs1057516792
HLIrs1057516792
Exacrs1057516792
Gnomadrs1057516792
Varsomers1057516792
LitVarrs1057516792
Maprs1057516792
PheGenIrs1057516792
Biobankrs1057516792
1000 genomesrs1057516792
hgdprs1057516792
ensemblrs1057516792
gopubmedrs1057516792
geneviewrs1057516792
scholarrs1057516792
googlers1057516792
pharmgkbrs1057516792
gwascentralrs1057516792
openSNPrs1057516792
23andMers1057516792
23andMe allrs1057516792
SNPshotrs1057516792
SNPdbers1057516792
MSV3drs1057516792
GWAS Ctlgrs1057516792
Max Magnitude0
ClinVar
Risk rs1057516792(-;-)
Alt rs1057516792(-;-)
Reference Rs1057516792(A;A)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C
Reversed 1
HGVS NC_000009.11:g.97897640delT
CLNSRC
CLNACC RCV000410893.1,