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rs397508034

From SNPedia

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


Make rs397508034(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379870
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508034
ClinGenrs397508034
ebirs397508034
HLIrs397508034
Exacrs397508034
Varsomers397508034
Maprs397508034
PheGenIrs397508034
hapmaprs397508034
1000 genomesrs397508034
hgdprs397508034
ensemblrs397508034
gopubmedrs397508034
geneviewrs397508034
scholarrs397508034
googlers397508034
pharmgkbrs397508034
gwascentralrs397508034
openSNPrs397508034
23andMers397508034
23andMe allrs397508034
SNP Nexus

SNPshotrs397508034
SNPdbers397508034
MSV3drs397508034
GWAS Ctlgrs397508034
Max Magnitude6
ClinVar
Risk rs397508034(-;-)
Alt rs397508034(-;-)
Reference Rs397508034(AT;AT)
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.32954007_32954008delTA
CLNSRC ClinVar
CLNACC RCV000045704.2, RCV000257553.2,