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rs397507851

From SNPedia

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


Make rs397507851(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340763
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507851
dbSNP (old)rs397507851
ClinGenrs397507851
ebirs397507851
HLIrs397507851
Exacrs397507851
Gnomadrs397507851
Varsomers397507851
Maprs397507851
PheGenIrs397507851
Biobankrs397507851
1000 genomesrs397507851
hgdprs397507851
ensemblrs397507851
gopubmedrs397507851
geneviewrs397507851
scholarrs397507851
googlers397507851
pharmgkbrs397507851
gwascentralrs397507851
openSNPrs397507851
23andMers397507851
23andMe allrs397507851
SNP Nexus

SNPshotrs397507851
SNPdbers397507851
MSV3drs397507851
GWAS Ctlgrs397507851
Max Magnitude6
ClinVar
Risk rs397507851(-;-)
Alt rs397507851(-;-)
Reference Rs397507851(TTAAATG;TTAAATG)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914900_32914906delAAATGTT
CLNSRC ClinVar
CLNACC RCV000044937.2, RCV000166653.2, RCV000241449.2,