Have questions? Visit https://www.reddit.com/r/SNPedia

rs730881614

From SNPedia

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


Make rs730881614(-;-)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32363181
GeneBRCA2
is asnp
is mentioned by
dbSNPrs730881614
dbSNP (old)rs730881614
ClinGenrs730881614
ebirs730881614
HLIrs730881614
Exacrs730881614
Varsomers730881614
Maprs730881614
PheGenIrs730881614
Biobankrs730881614
1000 genomesrs730881614
hgdprs730881614
ensemblrs730881614
gopubmedrs730881614
geneviewrs730881614
scholarrs730881614
googlers730881614
pharmgkbrs730881614
gwascentralrs730881614
openSNPrs730881614
23andMers730881614
23andMe allrs730881614
SNP Nexus

SNPshotrs730881614
SNPdbers730881614
MSV3drs730881614
GWAS Ctlgrs730881614
Max Magnitude6
ClinVar
Risk rs730881614(-;-)
Alt rs730881614(-;-)
Reference Rs730881614(ATATGATACGGAA;ATATGATACGGAA)
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.32937318_32937330delATGATACGGAAAT
CLNSRC
CLNACC RCV000160306.1, RCV000241464.1,