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rs781542763

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs781542763(A;A)
Make rs781542763(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position95171080
GeneFANCC
is asnp
is mentioned by
dbSNPrs781542763
ebirs781542763
HLIrs781542763
Exacrs781542763
Varsomers781542763
Maprs781542763
PheGenIrs781542763
hapmaprs781542763
1000 genomesrs781542763
hgdprs781542763
ensemblrs781542763
gopubmedrs781542763
geneviewrs781542763
scholarrs781542763
googlers781542763
pharmgkbrs781542763
gwascentralrs781542763
openSNPrs781542763
23andMers781542763
23andMe allrs781542763
SNP Nexus

SNPshotrs781542763
SNPdbers781542763
MSV3drs781542763
GWAS Ctlgrs781542763
Max Magnitude0
ClinVar
Risk rs781542763(A;A)
Alt rs781542763(A;A)
Reference rs781542763(G;G)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C
Reversed 0
HGVS NC_000009.11:g.97933362G>A
CLNSRC
CLNACC RCV000169411.1,