Have questions? Visit https://www.reddit.com/r/SNPedia

rs730881709

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881709(-;-)
Make rs730881709(-;T)
Make rs730881709(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position95111489
GeneC9orf3, FANCC
is asnp
is mentioned by
dbSNPrs730881709
ebirs730881709
HLIrs730881709
Exacrs730881709
Varsomers730881709
Maprs730881709
PheGenIrs730881709
hapmaprs730881709
1000 genomesrs730881709
hgdprs730881709
ensemblrs730881709
gopubmedrs730881709
geneviewrs730881709
scholarrs730881709
googlers730881709
pharmgkbrs730881709
gwascentralrs730881709
openSNPrs730881709
23andMers730881709
23andMe allrs730881709
SNP Nexus

SNPshotrs730881709
SNPdbers730881709
MSV3drs730881709
GWAS Ctlgrs730881709
Max Magnitude0
ClinVar
Risk rs730881709(T;T)
Alt rs730881709(T;T)
Reference rs730881709(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Fanconi anemia
Variation info
Gene FANCC
CLNDBN Hereditary cancer-predisposing syndrome Fanconi anemia
Reversed 1
HGVS NC_000009.11:g.97873772dupA
CLNSRC
CLNACC RCV000160468.1, RCV000203768.1,