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rs397507618

From SNPedia

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


Make rs397507618(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336505
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507618
dbSNP (old)rs397507618
ClinGenrs397507618
ebirs397507618
HLIrs397507618
Exacrs397507618
Gnomadrs397507618
Varsomers397507618
Maprs397507618
PheGenIrs397507618
Biobankrs397507618
1000 genomesrs397507618
hgdprs397507618
ensemblrs397507618
gopubmedrs397507618
geneviewrs397507618
scholarrs397507618
googlers397507618
pharmgkbrs397507618
gwascentralrs397507618
openSNPrs397507618
23andMers397507618
23andMe allrs397507618
SNP Nexus

SNPshotrs397507618
SNPdbers397507618
MSV3drs397507618
GWAS Ctlgrs397507618
Max Magnitude6
ClinVar
Risk rs397507618(-;-)
Alt rs397507618(-;-)
Reference Rs397507618(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer not provided
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 not provided
Reversed 0
HGVS NC_000013.10:g.32910642delG
CLNSRC ClinVar
CLNACC RCV000043951.2, RCV000241041.2, RCV000482272.1,