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rs886038147

From SNPedia

Merged intors80359587
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
(A;A) 0 common in clinvar


Make rs886038147(-;-)
ReferenceGRCh38.p7 38.3/149
Chromosome13
Position32340789
GeneBRCA2
is asnp
is mentioned by
dbSNPrs886038147
dbSNP (classic)rs886038147
ClinGenrs886038147
ebirs886038147
HLIrs886038147
Exacrs886038147
Gnomadrs886038147
Varsomers886038147
LitVarrs886038147
Maprs886038147
PheGenIrs886038147
Biobankrs886038147
1000 genomesrs886038147
hgdprs886038147
ensemblrs886038147
geneviewrs886038147
scholarrs886038147
googlers886038147
pharmgkbrs886038147
gwascentralrs886038147
openSNPrs886038147
23andMers886038147
23andMe allrs886038147
SNPshotrs886038147
SNPdbers886038147
MSV3drs886038147
GWAS Ctlgrs886038147
StatusMerged into rs80359587
Max Magnitude6
ClinVar
Risk
Alt
Reference Rs886038147(A;A)
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.32914926delA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044944.2, RCV000241168.3,