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rs587779909

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779909(A;A)
Make rs587779909(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position95135345
GeneC9orf3, FANCC
is asnp
is mentioned by
dbSNPrs587779909
ebirs587779909
HLIrs587779909
Exacrs587779909
Varsomers587779909
Maprs587779909
PheGenIrs587779909
hapmaprs587779909
1000 genomesrs587779909
hgdprs587779909
ensemblrs587779909
gopubmedrs587779909
geneviewrs587779909
scholarrs587779909
googlers587779909
pharmgkbrs587779909
gwascentralrs587779909
openSNPrs587779909
23andMers587779909
23andMe allrs587779909
SNP Nexus

SNPshotrs587779909
SNPdbers587779909
MSV3drs587779909
GWAS Ctlgrs587779909
Max Magnitude0
ClinVar
Risk rs587779909(A;A)
Alt rs587779909(A;A)
Reference rs587779909(G;G)
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.97897627C>T
CLNSRC
CLNACC RCV000115361.2, RCV000204814.1,