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rs397507906

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;G) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507906(-;-)
Make rs397507906(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355087
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507906
ebirs397507906
HLIrs397507906
Exacrs397507906
Varsomers397507906
Maprs397507906
PheGenIrs397507906
hapmaprs397507906
1000 genomesrs397507906
hgdprs397507906
ensemblrs397507906
gopubmedrs397507906
geneviewrs397507906
scholarrs397507906
googlers397507906
pharmgkbrs397507906
gwascentralrs397507906
openSNPrs397507906
23andMers397507906
23andMe allrs397507906
SNP Nexus

SNPshotrs397507906
SNPdbers397507906
MSV3drs397507906
GWAS Ctlgrs397507906
Max Magnitude6
rs397507906, also known as 7463insG, c.7234_7235insG and p.Thr2412Serfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs397507906(G;G)
Alt rs397507906(G;G)
Reference rs397507906(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32929224_32929225insG
CLNSRC ClinVar
CLNACC RCV000045172.2,