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rs397507559

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAGGTGTTTT;GAGGTGTTTT) 0 common in clinvar
Make rs397507559(-;-)
Make rs397507559(-;GAGGTGTTTT)
ReferenceGRCh38 38.1/141
Chromosome9
Position35075706
GeneFANCG
is asnp
is mentioned by
dbSNPrs397507559
ebirs397507559
HLIrs397507559
Exacrs397507559
Varsomers397507559
Maprs397507559
PheGenIrs397507559
hapmaprs397507559
1000 genomesrs397507559
hgdprs397507559
ensemblrs397507559
gopubmedrs397507559
geneviewrs397507559
scholarrs397507559
googlers397507559
pharmgkbrs397507559
gwascentralrs397507559
openSNPrs397507559
23andMers397507559
23andMe allrs397507559
SNP Nexus

SNPshotrs397507559
SNPdbers397507559
MSV3drs397507559
GWAS Ctlgrs397507559
Max Magnitude0
ClinVar
Risk rs397507559(;)
Alt rs397507559(;)
Reference rs397507559(GAGGTGTTTT;GAGGTGTTTT)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCG
CLNDBN Fanconi anemia, complementation group G
Reversed 1
HGVS NC_000009.11:g.35075703_35075712delAAAACACCTC
CLNSRC ClinVar GeneReviews
CLNACC RCV000034123.2,