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rs864622568

From SNPedia

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


Make rs864622568(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32379823
GeneBRCA2
is asnp
is mentioned by
dbSNPrs864622568
dbSNP (classic)rs864622568
ClinGenrs864622568
ebirs864622568
HLIrs864622568
Exacrs864622568
Gnomadrs864622568
Varsomers864622568
LitVarrs864622568
Maprs864622568
PheGenIrs864622568
Biobankrs864622568
1000 genomesrs864622568
hgdprs864622568
ensemblrs864622568
geneviewrs864622568
scholarrs864622568
googlers864622568
pharmgkbrs864622568
gwascentralrs864622568
openSNPrs864622568
23andMers864622568
SNPshotrs864622568
SNPdbers864622568
MSV3drs864622568
GWAS Ctlgrs864622568
Max Magnitude6
ClinVar
Risk rs864622568(G;G)
Alt rs864622568(G;G)
Reference Rs864622568(T;T)
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.32953960T>G
CLNSRC
CLNACC RCV000205381.2, RCV000240965.1,