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rs730882168

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730882168(-;-)
Make rs730882168(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32339745
GeneBRCA2
is asnp
is mentioned by
dbSNPrs730882168
ebirs730882168
HLIrs730882168
Exacrs730882168
Varsomers730882168
Maprs730882168
PheGenIrs730882168
hapmaprs730882168
1000 genomesrs730882168
hgdprs730882168
ensemblrs730882168
gopubmedrs730882168
geneviewrs730882168
scholarrs730882168
googlers730882168
pharmgkbrs730882168
gwascentralrs730882168
openSNPrs730882168
23andMers730882168
23andMe allrs730882168
SNP Nexus

SNPshotrs730882168
SNPdbers730882168
MSV3drs730882168
GWAS Ctlgrs730882168
Max Magnitude0
ClinVar
Risk rs730882168(;)
Alt rs730882168(;)
Reference rs730882168(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913882delC
CLNSRC
CLNACC RCV000162055.1,