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rs587779898

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779898(A;G)
Make rs587779898(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position95249371
GeneFANCC
is asnp
is mentioned by
dbSNPrs587779898
ebirs587779898
HLIrs587779898
Exacrs587779898
Varsomers587779898
Maprs587779898
PheGenIrs587779898
hapmaprs587779898
1000 genomesrs587779898
hgdprs587779898
ensemblrs587779898
gopubmedrs587779898
geneviewrs587779898
scholarrs587779898
googlers587779898
pharmgkbrs587779898
gwascentralrs587779898
openSNPrs587779898
23andMers587779898
23andMe allrs587779898
SNP Nexus

SNPshotrs587779898
SNPdbers587779898
MSV3drs587779898
GWAS Ctlgrs587779898
Max Magnitude0
ClinVar
Risk rs587779898(G;G)
Alt rs587779898(G;G)
Reference rs587779898(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FANCC
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.98011653T>C
CLNSRC
CLNACC RCV000115337.3,