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rs863224441

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224441(G;G)
Make rs863224441(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position95126527
GeneC9orf3, FANCC
is asnp
is mentioned by
dbSNPrs863224441
ebirs863224441
HLIrs863224441
Exacrs863224441
Varsomers863224441
Maprs863224441
PheGenIrs863224441
hapmaprs863224441
1000 genomesrs863224441
hgdprs863224441
ensemblrs863224441
gopubmedrs863224441
geneviewrs863224441
scholarrs863224441
googlers863224441
pharmgkbrs863224441
gwascentralrs863224441
openSNPrs863224441
23andMers863224441
23andMe allrs863224441
SNP Nexus

SNPshotrs863224441
SNPdbers863224441
MSV3drs863224441
GWAS Ctlgrs863224441
Max Magnitude0
ClinVar
Risk rs863224441(G;G)
Alt rs863224441(G;G)
Reference rs863224441(T;T)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia
Reversed 1
HGVS NC_000009.11:g.97888809A>C
CLNSRC
CLNACC RCV000196695.1,