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rs1057516384

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057516384(C;T)
Make rs1057516384(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95240687
GeneFANCC
is asnp
is mentioned by
dbSNPrs1057516384
dbSNP (old)rs1057516384
ClinGenrs1057516384
ebirs1057516384
HLIrs1057516384
Exacrs1057516384
Gnomadrs1057516384
Varsomers1057516384
LitVarrs1057516384
Maprs1057516384
PheGenIrs1057516384
Biobankrs1057516384
1000 genomesrs1057516384
hgdprs1057516384
ensemblrs1057516384
gopubmedrs1057516384
geneviewrs1057516384
scholarrs1057516384
googlers1057516384
pharmgkbrs1057516384
gwascentralrs1057516384
openSNPrs1057516384
23andMers1057516384
23andMe allrs1057516384
SNPshotrs1057516384
SNPdbers1057516384
MSV3drs1057516384
GWAS Ctlgrs1057516384
Max Magnitude0
ClinVar
Risk rs1057516384(T;T)
Alt rs1057516384(T;T)
Reference Rs1057516384(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.98002969G>A
CLNSRC
CLNACC RCV000412276.1,