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rs121434426

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434426(C;T)
Make rs121434426(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position35076442
GeneFANCG
is asnp
is mentioned by
dbSNPrs121434426
ebirs121434426
HLIrs121434426
Exacrs121434426
Varsomers121434426
Maprs121434426
PheGenIrs121434426
hapmaprs121434426
1000 genomesrs121434426
hgdprs121434426
ensemblrs121434426
gopubmedrs121434426
geneviewrs121434426
scholarrs121434426
googlers121434426
pharmgkbrs121434426
gwascentralrs121434426
openSNPrs121434426
23andMers121434426
23andMe allrs121434426
SNP Nexus

SNPshotrs121434426
SNPdbers121434426
MSV3drs121434426
GWAS Ctlgrs121434426
Max Magnitude0
OMIM602956
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121434426(T;T)
Alt rs121434426(T;T)
Reference rs121434426(C;C)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCG
CLNDBN Fanconi anemia, complementation group G
Reversed 1
HGVS NC_000009.11:g.35076439G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007107.2,