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rs886040671

From SNPedia

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


Make rs886040671(-;-)
ReferenceGRCh38.p7 38.3/149
Chromosome13
Position32329475
GeneBRCA2
is asnp
is mentioned by
dbSNPrs886040671
dbSNP (classic)rs886040671
ClinGenrs886040671
ebirs886040671
HLIrs886040671
Exacrs886040671
Gnomadrs886040671
Varsomers886040671
LitVarrs886040671
Maprs886040671
PheGenIrs886040671
Biobankrs886040671
1000 genomesrs886040671
hgdprs886040671
ensemblrs886040671
geneviewrs886040671
scholarrs886040671
googlers886040671
pharmgkbrs886040671
gwascentralrs886040671
openSNPrs886040671
23andMers886040671
23andMe allrs886040671
SNPshotrs886040671
SNPdbers886040671
MSV3drs886040671
GWAS Ctlgrs886040671
Max Magnitude6
ClinVar
Risk rs886040671(-;-)
Alt rs886040671(-;-)
Reference Rs886040671(CC;CC)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32903612_32903613delCC
CLNSRC
CLNACC RCV000256576.1,