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rs886038161

From SNPedia

Merged intors80359638
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;AA) 6 BRCA2 variant considered pathogenic for breast cancer
(AA;AA) 0 common in clinvar


Make rs886038161(-;-)
ReferenceGRCh38.p7 38.3/149
Chromosome13
Position32354962
GeneBRCA2
is asnp
is mentioned by
dbSNPrs886038161
dbSNP (classic)rs886038161
ClinGenrs886038161
ebirs886038161
HLIrs886038161
Exacrs886038161
Gnomadrs886038161
Varsomers886038161
LitVarrs886038161
Maprs886038161
PheGenIrs886038161
Biobankrs886038161
1000 genomesrs886038161
hgdprs886038161
ensemblrs886038161
geneviewrs886038161
scholarrs886038161
googlers886038161
pharmgkbrs886038161
gwascentralrs886038161
openSNPrs886038161
23andMers886038161
23andMe allrs886038161
SNPshotrs886038161
SNPdbers886038161
MSV3drs886038161
GWAS Ctlgrs886038161
StatusMerged into rs80359638
Max Magnitude6
ClinVar
Risk
Alt
Reference Rs886038161(AA;AA)
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.32929099_32929100delAA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045144.2, RCV000241365.3,