Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507561

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507561(A;G)
Make rs397507561(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position35076585
GeneFANCG
is asnp
is mentioned by
dbSNPrs397507561
ebirs397507561
HLIrs397507561
Exacrs397507561
Varsomers397507561
Maprs397507561
PheGenIrs397507561
hapmaprs397507561
1000 genomesrs397507561
hgdprs397507561
ensemblrs397507561
gopubmedrs397507561
geneviewrs397507561
scholarrs397507561
googlers397507561
pharmgkbrs397507561
gwascentralrs397507561
openSNPrs397507561
23andMers397507561
23andMe allrs397507561
SNP Nexus

SNPshotrs397507561
SNPdbers397507561
MSV3drs397507561
GWAS Ctlgrs397507561
Max Magnitude0
ClinVar
Risk rs397507561(G;G)
Alt rs397507561(G;G)
Reference rs397507561(A;A)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCG
CLNDBN Fanconi anemia, complementation group G
Reversed 1
HGVS NC_000009.11:g.35076582T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007108.3,