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rs730881620

From SNPedia

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Geno Mag Summary
(AAGA;AAGA) 0 common in clinvar
Make rs730881620(-;-)
Make rs730881620(-;AAGA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32338175
GeneBRCA2
is asnp
is mentioned by
dbSNPrs730881620
ebirs730881620
HLIrs730881620
Exacrs730881620
Varsomers730881620
Maprs730881620
PheGenIrs730881620
hapmaprs730881620
1000 genomesrs730881620
hgdprs730881620
ensemblrs730881620
gopubmedrs730881620
geneviewrs730881620
scholarrs730881620
googlers730881620
pharmgkbrs730881620
gwascentralrs730881620
openSNPrs730881620
23andMers730881620
23andMe allrs730881620
SNP Nexus

SNPshotrs730881620
SNPdbers730881620
MSV3drs730881620
GWAS Ctlgrs730881620
Max Magnitude0
ClinVar
Risk rs730881620(;)
Alt rs730881620(;)
Reference rs730881620(AAGA;AAGA)
Significance Pathogenic
Disease Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32912312_32912315delAAGA
CLNSRC
CLNACC RCV000160315.1, RCV000217692.1,