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rs200479612

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200479612(C;G)
Make rs200479612(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position35078604
GeneFANCG
is asnp
is mentioned by
dbSNPrs200479612
ebirs200479612
HLIrs200479612
Exacrs200479612
Varsomers200479612
Maprs200479612
PheGenIrs200479612
hapmaprs200479612
1000 genomesrs200479612
hgdprs200479612
ensemblrs200479612
gopubmedrs200479612
geneviewrs200479612
scholarrs200479612
googlers200479612
pharmgkbrs200479612
gwascentralrs200479612
openSNPrs200479612
23andMers200479612
23andMe allrs200479612
SNP Nexus

SNPshotrs200479612
SNPdbers200479612
MSV3drs200479612
GWAS Ctlgrs200479612
Max Magnitude0
ClinVar
Risk rs200479612(G,T;G,T)
Alt rs200479612(G,T;G,T)
Reference rs200479612(C;C)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCG
CLNDBN Fanconi anemia, complementation group G
Reversed 0
HGVS NC_000009.11:g.35078601C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007106.3,