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rs397507607

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;TTATA) 6 BRCA2 variant considered pathogenic for breast cancer
(TTATA;TTATA) 0 common in clinvar


Make rs397507607(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333275
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507607
ClinGenrs397507607
ebirs397507607
HLIrs397507607
Exacrs397507607
Varsomers397507607
Maprs397507607
PheGenIrs397507607
hapmaprs397507607
1000 genomesrs397507607
hgdprs397507607
ensemblrs397507607
gopubmedrs397507607
geneviewrs397507607
scholarrs397507607
googlers397507607
pharmgkbrs397507607
gwascentralrs397507607
openSNPrs397507607
23andMers397507607
23andMe allrs397507607
SNP Nexus

SNPshotrs397507607
SNPdbers397507607
MSV3drs397507607
GWAS Ctlgrs397507607
Max Magnitude6
ClinVar
Risk rs397507607(-;-)
Alt rs397507607(-;-)
Reference Rs397507607(TTATA;TTATA)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32907412_32907416delTTATA
CLNSRC ClinVar
CLNACC RCV000043888.3, RCV000256566.2,