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rs769039987

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs769039987(A;A)
Make rs769039987(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position95150074
GeneFANCC
is asnp
is mentioned by
dbSNPrs769039987
ebirs769039987
HLIrs769039987
Exacrs769039987
Varsomers769039987
Maprs769039987
PheGenIrs769039987
hapmaprs769039987
1000 genomesrs769039987
hgdprs769039987
ensemblrs769039987
gopubmedrs769039987
geneviewrs769039987
scholarrs769039987
googlers769039987
pharmgkbrs769039987
gwascentralrs769039987
openSNPrs769039987
23andMers769039987
23andMe allrs769039987
SNP Nexus

SNPshotrs769039987
SNPdbers769039987
MSV3drs769039987
GWAS Ctlgrs769039987
Max Magnitude0
ClinVar
Risk rs769039987(A;A)
Alt rs769039987(A;A)
Reference rs769039987(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FANCC
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.97912356G>A
CLNSRC
CLNACC RCV000224844.1,