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rs397507552

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TTGG;TTGG) 0 common in clinvar
Make rs397507552(-;-)
Make rs397507552(-;TTGG)
ReferenceGRCh38 38.1/141
Chromosome16
Position89792034
GeneFANCA
is asnp
is mentioned by
dbSNPrs397507552
ebirs397507552
HLIrs397507552
Exacrs397507552
Varsomers397507552
Maprs397507552
PheGenIrs397507552
hapmaprs397507552
1000 genomesrs397507552
hgdprs397507552
ensemblrs397507552
gopubmedrs397507552
geneviewrs397507552
scholarrs397507552
googlers397507552
pharmgkbrs397507552
gwascentralrs397507552
openSNPrs397507552
23andMers397507552
23andMe allrs397507552
SNP Nexus

SNPshotrs397507552
SNPdbers397507552
MSV3drs397507552
GWAS Ctlgrs397507552
Max Magnitude0
ClinVar
Risk rs397507552(;)
Alt rs397507552(;)
Reference rs397507552(TTGG;TTGG)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia, complementation group A
Reversed 1
HGVS NC_000016.9:g.89858442_89858445delCCAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000003609.4,