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rs730881612

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881612(-;-)
Make rs730881612(-;G)
Make rs730881612(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32355233
GeneBRCA2
is asnp
is mentioned by
dbSNPrs730881612
ebirs730881612
HLIrs730881612
Exacrs730881612
Varsomers730881612
Maprs730881612
PheGenIrs730881612
hapmaprs730881612
1000 genomesrs730881612
hgdprs730881612
ensemblrs730881612
gopubmedrs730881612
geneviewrs730881612
scholarrs730881612
googlers730881612
pharmgkbrs730881612
gwascentralrs730881612
openSNPrs730881612
23andMers730881612
23andMe allrs730881612
SNP Nexus

SNPshotrs730881612
SNPdbers730881612
MSV3drs730881612
GWAS Ctlgrs730881612
Max Magnitude0
ClinVar
Risk rs730881612(G;G)
Alt rs730881612(G;G)
Reference rs730881612(;)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32929370_32929371insG
CLNSRC
CLNACC RCV000160304.1,