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rs121434425

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434425(G;T)
Make rs121434425(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position35078338
GeneFANCG
is asnp
is mentioned by
dbSNPrs121434425
ebirs121434425
HLIrs121434425
Exacrs121434425
Varsomers121434425
Maprs121434425
PheGenIrs121434425
hapmaprs121434425
1000 genomesrs121434425
hgdprs121434425
ensemblrs121434425
gopubmedrs121434425
geneviewrs121434425
scholarrs121434425
googlers121434425
pharmgkbrs121434425
gwascentralrs121434425
openSNPrs121434425
23andMers121434425
23andMe allrs121434425
SNP Nexus

SNPshotrs121434425
SNPdbers121434425
MSV3drs121434425
GWAS Ctlgrs121434425
Max Magnitude0
OMIM602956
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434425(T;T)
Alt rs121434425(T;T)
Reference rs121434425(G;G)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCG
CLNDBN Fanconi anemia, complementation group G
Reversed 1
HGVS NC_000009.11:g.35078335C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007104.2,