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rs397507560

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTGGATCCGT;CTGGATCCGT) 0 common in clinvar
(TGGATCCGTC;TGGATCCGTC) 0 common in clinvar
Make rs397507560(-;-)
Make rs397507560(-;CTGGATCCGT)
ReferenceGRCh38 38.1/141
Chromosome9
Position35074174
GeneFANCG, VCP
is asnp
is mentioned by
dbSNPrs397507560
dbSNP (old)rs397507560
ClinGenrs397507560
ebirs397507560
HLIrs397507560
Exacrs397507560
Gnomadrs397507560
Varsomers397507560
Maprs397507560
PheGenIrs397507560
Biobankrs397507560
1000 genomesrs397507560
hgdprs397507560
ensemblrs397507560
gopubmedrs397507560
geneviewrs397507560
scholarrs397507560
googlers397507560
pharmgkbrs397507560
gwascentralrs397507560
openSNPrs397507560
23andMers397507560
23andMe allrs397507560
SNP Nexus

SNPshotrs397507560
SNPdbers397507560
MSV3drs397507560
GWAS Ctlgrs397507560
Max Magnitude0
ClinVar
Risk Rs397507560(TGGATCCGTC;TGGATCCGTC) rs397507560(-;-)
Alt Rs397507560(TGGATCCGTC;TGGATCCGTC) rs397507560(-;-)
Reference Rs397507560(CTGGATCCGT;CTGGATCCGT)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene VCP FANCG
CLNDBN Fanconi anemia, complementation group G
Reversed 1
HGVS NC_000009.11:g.35074171_35074180delACGGATCCAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000007110.3,