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rs1057516291

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516291(A;A)
Make rs1057516291(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95240655
GeneFANCC
is asnp
is mentioned by
dbSNPrs1057516291
dbSNP (old)rs1057516291
ClinGenrs1057516291
ebirs1057516291
HLIrs1057516291
Exacrs1057516291
Gnomadrs1057516291
Varsomers1057516291
Maprs1057516291
PheGenIrs1057516291
Biobankrs1057516291
1000 genomesrs1057516291
hgdprs1057516291
ensemblrs1057516291
gopubmedrs1057516291
geneviewrs1057516291
scholarrs1057516291
googlers1057516291
pharmgkbrs1057516291
gwascentralrs1057516291
openSNPrs1057516291
23andMers1057516291
23andMe allrs1057516291
SNPshotrs1057516291
SNPdbers1057516291
MSV3drs1057516291
GWAS Ctlgrs1057516291
Max Magnitude0
ClinVar
Risk rs1057516291(A;A)
Alt rs1057516291(A;A)
Reference Rs1057516291(G;G)
Significance Pathogenic
Disease Fanconi anemia Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C Fanconi anemia
Reversed 1
HGVS NC_000009.11:g.98002937C>T
CLNSRC
CLNACC RCV000412313.1, RCV000462409.1,