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rs587779904

From SNPedia

Orientationminus
Geno Mag Summary
(TCTCAT;TCTCAT) 0 common in clinvar
Make rs587779904(A;A)
Make rs587779904(A;TCTCAT)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position95172133
GeneFANCC
is asnp
is mentioned by
dbSNPrs587779904
ebirs587779904
HLIrs587779904
Exacrs587779904
Varsomers587779904
Maprs587779904
PheGenIrs587779904
hapmaprs587779904
1000 genomesrs587779904
hgdprs587779904
ensemblrs587779904
gopubmedrs587779904
geneviewrs587779904
scholarrs587779904
googlers587779904
pharmgkbrs587779904
gwascentralrs587779904
openSNPrs587779904
23andMers587779904
23andMe allrs587779904
SNP Nexus

SNPshotrs587779904
SNPdbers587779904
MSV3drs587779904
GWAS Ctlgrs587779904
Max Magnitude0
ClinVar
Risk rs587779904(A;A)
Alt rs587779904(A;A)
Reference rs587779904(TCTCAT;TCTCAT)
Significance Pathogenic
Disease not provided Fanconi anemia
Variation info
Gene FANCC
CLNDBN not provided Fanconi anemia
Reversed 1
HGVS NC_000009.11:g.97934415_97934420delATGAGAinsT
CLNSRC
CLNACC RCV000115350.3, RCV000229758.1,