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rs794726668

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794726668(G;T)
Make rs794726668(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position95249126
GeneFANCC
is asnp
is mentioned by
dbSNPrs794726668
ebirs794726668
HLIrs794726668
Exacrs794726668
Varsomers794726668
Maprs794726668
PheGenIrs794726668
hapmaprs794726668
1000 genomesrs794726668
hgdprs794726668
ensemblrs794726668
gopubmedrs794726668
geneviewrs794726668
scholarrs794726668
googlers794726668
pharmgkbrs794726668
gwascentralrs794726668
openSNPrs794726668
23andMers794726668
23andMe allrs794726668
SNP Nexus

SNPshotrs794726668
SNPdbers794726668
MSV3drs794726668
GWAS Ctlgrs794726668
Max Magnitude0
ClinVar
Risk rs794726668(T;T)
Alt rs794726668(T;T)
Reference rs794726668(G;G)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C
Reversed 1
HGVS NC_000009.11:g.98011408C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012831.3,