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rs864622609

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs864622609(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32337546
GeneBRCA2
is asnp
is mentioned by
dbSNPrs864622609
dbSNP (old)rs864622609
ClinGenrs864622609
ebirs864622609
HLIrs864622609
Exacrs864622609
Varsomers864622609
Maprs864622609
PheGenIrs864622609
Biobankrs864622609
1000 genomesrs864622609
hgdprs864622609
ensemblrs864622609
gopubmedrs864622609
geneviewrs864622609
scholarrs864622609
googlers864622609
pharmgkbrs864622609
gwascentralrs864622609
openSNPrs864622609
23andMers864622609
23andMe allrs864622609
SNP Nexus

SNPshotrs864622609
SNPdbers864622609
MSV3drs864622609
GWAS Ctlgrs864622609
Max Magnitude6
ClinVar
Risk rs864622609(A;A) rs864622609(G;G)
Alt rs864622609(A;A) rs864622609(G;G)
Reference Rs864622609(C;C)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911683C>A; NC_000013.10:g.32911683C>G
CLNSRC
CLNACC RCV000456624.1, RCV000204433.1, RCV000241250.1,