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rs863224827

From SNPedia

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


Make rs863224827(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32338870
GeneBRCA2
is asnp
is mentioned by
dbSNPrs863224827
dbSNP (old)rs863224827
ClinGenrs863224827
ebirs863224827
HLIrs863224827
Exacrs863224827
Gnomadrs863224827
Varsomers863224827
Maprs863224827
PheGenIrs863224827
Biobankrs863224827
1000 genomesrs863224827
hgdprs863224827
ensemblrs863224827
gopubmedrs863224827
geneviewrs863224827
scholarrs863224827
googlers863224827
pharmgkbrs863224827
gwascentralrs863224827
openSNPrs863224827
23andMers863224827
23andMe allrs863224827
SNP Nexus

SNPshotrs863224827
SNPdbers863224827
MSV3drs863224827
GWAS Ctlgrs863224827
Max Magnitude6
ClinVar
Risk rs863224827(-;-)
Alt rs863224827(-;-)
Reference Rs863224827(GACCTTCCAGG;GACCTTCCAGG)
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.32913007_32913017delCTTCCAGGGAC
CLNSRC
CLNACC RCV000199893.1, RCV000240973.1,