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rs730881602

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881602(-;-)
Make rs730881602(-;A)
Make rs730881602(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32336735
GeneBRCA2
is asnp
is mentioned by
dbSNPrs730881602
ebirs730881602
HLIrs730881602
Exacrs730881602
Varsomers730881602
Maprs730881602
PheGenIrs730881602
hapmaprs730881602
1000 genomesrs730881602
hgdprs730881602
ensemblrs730881602
gopubmedrs730881602
geneviewrs730881602
scholarrs730881602
googlers730881602
pharmgkbrs730881602
gwascentralrs730881602
openSNPrs730881602
23andMers730881602
23andMe allrs730881602
SNP Nexus

SNPshotrs730881602
SNPdbers730881602
MSV3drs730881602
GWAS Ctlgrs730881602
Max Magnitude0
ClinVar
Risk rs730881602(A;A)
Alt rs730881602(A;A)
Reference rs730881602(;)
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.32910872dupA
CLNSRC
CLNACC RCV000160271.1, RCV000238934.1,