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rs397507918

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507918(-;-)
Make rs397507918(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32356459
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507918
ebirs397507918
HLIrs397507918
Exacrs397507918
Varsomers397507918
Maprs397507918
PheGenIrs397507918
hapmaprs397507918
1000 genomesrs397507918
hgdprs397507918
ensemblrs397507918
gopubmedrs397507918
geneviewrs397507918
scholarrs397507918
googlers397507918
pharmgkbrs397507918
gwascentralrs397507918
openSNPrs397507918
23andMers397507918
23andMe allrs397507918
SNP Nexus

SNPshotrs397507918
SNPdbers397507918
MSV3drs397507918
GWAS Ctlgrs397507918
Max Magnitude6
rs397507918, also known as 7696insT, c.7467_7468insT and p.Ile2490TyrfsX7, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs397507918(T;T)
Alt rs397507918(T;T)
Reference rs397507918(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32930596dupT
CLNSRC ClinVar
CLNACC RCV000045224.2,