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rs1057516488

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516488(A;A)
Make rs1057516488(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95107082
GeneC9orf3, FANCC, LOC107987102
is asnp
is mentioned by
dbSNPrs1057516488
dbSNP (old)rs1057516488
ClinGenrs1057516488
ebirs1057516488
HLIrs1057516488
Exacrs1057516488
Gnomadrs1057516488
Varsomers1057516488
Maprs1057516488
PheGenIrs1057516488
Biobankrs1057516488
1000 genomesrs1057516488
hgdprs1057516488
ensemblrs1057516488
gopubmedrs1057516488
geneviewrs1057516488
scholarrs1057516488
googlers1057516488
pharmgkbrs1057516488
gwascentralrs1057516488
openSNPrs1057516488
23andMers1057516488
23andMe allrs1057516488
SNPshotrs1057516488
SNPdbers1057516488
MSV3drs1057516488
GWAS Ctlgrs1057516488
Max Magnitude0
ClinVar
Risk rs1057516488(A;A)
Alt rs1057516488(A;A)
Reference Rs1057516488(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.97869364C>T
CLNSRC
CLNACC RCV000409398.1,