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rs863224506

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863224506(-;G)
Make rs863224506(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position35079169
GeneFANCG
is asnp
is mentioned by
dbSNPrs863224506
ClinGenrs863224506
ebirs863224506
HLIrs863224506
Exacrs863224506
Varsomers863224506
Maprs863224506
PheGenIrs863224506
hapmaprs863224506
1000 genomesrs863224506
hgdprs863224506
ensemblrs863224506
gopubmedrs863224506
geneviewrs863224506
scholarrs863224506
googlers863224506
pharmgkbrs863224506
gwascentralrs863224506
openSNPrs863224506
23andMers863224506
23andMe allrs863224506
SNP Nexus

SNPshotrs863224506
SNPdbers863224506
MSV3drs863224506
GWAS Ctlgrs863224506
Max Magnitude0
ClinVar
Risk rs863224506(G;G)
Alt rs863224506(G;G)
Reference Rs863224506(-;-)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCG
CLNDBN Fanconi anemia
Reversed 1
HGVS NC_000009.11:g.35079167dupC
CLNSRC
CLNACC RCV000198686.3,