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rs397507664

From SNPedia

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


Make rs397507664(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337707
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507664
ClinGenrs397507664
ebirs397507664
HLIrs397507664
Exacrs397507664
Varsomers397507664
Maprs397507664
PheGenIrs397507664
hapmaprs397507664
1000 genomesrs397507664
hgdprs397507664
ensemblrs397507664
gopubmedrs397507664
geneviewrs397507664
scholarrs397507664
googlers397507664
pharmgkbrs397507664
gwascentralrs397507664
openSNPrs397507664
23andMers397507664
23andMe allrs397507664
SNP Nexus

SNPshotrs397507664
SNPdbers397507664
MSV3drs397507664
GWAS Ctlgrs397507664
Max Magnitude6
ClinVar
Risk rs397507664(-;-)
Alt rs397507664(-;-)
Reference Rs397507664(ATTAG;ATTAG)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911844_32911848delTTAGA
CLNSRC ClinVar
CLNACC RCV000044179.2, RCV000257058.2,