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rs1057516963

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516963(G;T)
Make rs1057516963(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95107101
GeneC9orf3, FANCC, LOC107987102
is asnp
is mentioned by
dbSNPrs1057516963
dbSNP (old)rs1057516963
ClinGenrs1057516963
ebirs1057516963
HLIrs1057516963
Exacrs1057516963
Gnomadrs1057516963
Varsomers1057516963
LitVarrs1057516963
Maprs1057516963
PheGenIrs1057516963
Biobankrs1057516963
1000 genomesrs1057516963
hgdprs1057516963
ensemblrs1057516963
gopubmedrs1057516963
geneviewrs1057516963
scholarrs1057516963
googlers1057516963
pharmgkbrs1057516963
gwascentralrs1057516963
openSNPrs1057516963
23andMers1057516963
23andMe allrs1057516963
SNPshotrs1057516963
SNPdbers1057516963
MSV3drs1057516963
GWAS Ctlgrs1057516963
Max Magnitude0
ClinVar
Risk rs1057516963(T;T)
Alt rs1057516963(T;T)
Reference Rs1057516963(G;G)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C
Reversed 1
HGVS NC_000009.11:g.97869383C>A
CLNSRC
CLNACC RCV000409084.1,