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rs794726667

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794726667(-;A)
Make rs794726667(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position95101828
GeneC9orf3, FANCC
is asnp
is mentioned by
dbSNPrs794726667
ClinGenrs794726667
ebirs794726667
HLIrs794726667
Exacrs794726667
Varsomers794726667
Maprs794726667
PheGenIrs794726667
hapmaprs794726667
1000 genomesrs794726667
hgdprs794726667
ensemblrs794726667
gopubmedrs794726667
geneviewrs794726667
scholarrs794726667
googlers794726667
pharmgkbrs794726667
gwascentralrs794726667
openSNPrs794726667
23andMers794726667
23andMe allrs794726667
SNP Nexus

SNPshotrs794726667
SNPdbers794726667
MSV3drs794726667
GWAS Ctlgrs794726667
Max Magnitude0
ClinVar
Risk rs794726667(A;A)
Alt rs794726667(A;A)
Reference Rs794726667(;)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C
Reversed 1
HGVS NC_000009.11:g.97864111dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000012828.3,