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rs397507625

From SNPedia

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


Make rs397507625(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336757
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507625
ClinGenrs397507625
ebirs397507625
HLIrs397507625
Exacrs397507625
Varsomers397507625
Maprs397507625
PheGenIrs397507625
hapmaprs397507625
1000 genomesrs397507625
hgdprs397507625
ensemblrs397507625
gopubmedrs397507625
geneviewrs397507625
scholarrs397507625
googlers397507625
pharmgkbrs397507625
gwascentralrs397507625
openSNPrs397507625
23andMers397507625
23andMe allrs397507625
SNP Nexus

SNPshotrs397507625
SNPdbers397507625
MSV3drs397507625
GWAS Ctlgrs397507625
Max Magnitude6
ClinVar
Risk rs397507625(-;-)
Alt rs397507625(-;-)
Reference Rs397507625(AACAATTATGA;AACAATTATGA)
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.32910894_32910904delACAATTATGAA
CLNSRC ClinVar
CLNACC RCV000043983.2, RCV000257653.2,