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rs864622735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACCGTGTGGAAG;ACCGTGTGGAAG) 0 common in clinvar
(ACCGTGTGGAAG;TCCC) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs864622735(TCCC;TCCC)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32379464
GeneBRCA2
is asnp
is mentioned by
dbSNPrs864622735
ClinGenrs864622735
ebirs864622735
HLIrs864622735
Exacrs864622735
Varsomers864622735
Maprs864622735
PheGenIrs864622735
hapmaprs864622735
1000 genomesrs864622735
hgdprs864622735
ensemblrs864622735
gopubmedrs864622735
geneviewrs864622735
scholarrs864622735
googlers864622735
pharmgkbrs864622735
gwascentralrs864622735
openSNPrs864622735
23andMers864622735
23andMe allrs864622735
SNP Nexus

SNPshotrs864622735
SNPdbers864622735
MSV3drs864622735
GWAS Ctlgrs864622735
Max Magnitude6
ClinVar
Risk rs864622735(TCCC;TCCC)
Alt rs864622735(TCCC;TCCC)
Reference Rs864622735(ACCGTGTGGAAG;ACCGTGTGGAAG)
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.32953601_32953612delACCGTGTGGAAGinsTCCC
CLNSRC
CLNACC RCV000204579.1, RCV000225419.1,