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rs398122599

From SNPedia

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


Make rs398122599(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363402
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122599
dbSNP (old)rs398122599
ClinGenrs398122599
ebirs398122599
HLIrs398122599
Exacrs398122599
Gnomadrs398122599
Varsomers398122599
Maprs398122599
PheGenIrs398122599
Biobankrs398122599
1000 genomesrs398122599
hgdprs398122599
ensemblrs398122599
gopubmedrs398122599
geneviewrs398122599
scholarrs398122599
googlers398122599
pharmgkbrs398122599
gwascentralrs398122599
openSNPrs398122599
23andMers398122599
23andMe allrs398122599
SNP Nexus

SNPshotrs398122599
SNPdbers398122599
MSV3drs398122599
GWAS Ctlgrs398122599
Max Magnitude6
ClinVar
Risk rs398122599(-;-)
Alt rs398122599(-;-)
Reference Rs398122599(TCCTCCCCTC;TCCTCCCCTC)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32937539_32937548delCCTCCCCTCT
CLNSRC ClinVar
CLNACC RCV000077021.3,