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rs1057516917

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516917(G;T)
Make rs1057516917(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95171144
GeneFANCC
is asnp
is mentioned by
dbSNPrs1057516917
dbSNP (classic)rs1057516917
ClinGenrs1057516917
ebirs1057516917
HLIrs1057516917
Exacrs1057516917
Gnomadrs1057516917
Varsomers1057516917
LitVarrs1057516917
Maprs1057516917
PheGenIrs1057516917
Biobankrs1057516917
1000 genomesrs1057516917
hgdprs1057516917
ensemblrs1057516917
geneviewrs1057516917
scholarrs1057516917
googlers1057516917
pharmgkbrs1057516917
gwascentralrs1057516917
openSNPrs1057516917
23andMers1057516917
23andMe allrs1057516917
SNPshotrs1057516917
SNPdbers1057516917
MSV3drs1057516917
GWAS Ctlgrs1057516917
Max Magnitude0
ClinVar
Risk rs1057516917(T;T)
Alt rs1057516917(T;T)
Reference Rs1057516917(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.97933426C>A
CLNSRC
CLNACC RCV000410360.1,