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rs730881604

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881604(-;-)
Make rs730881604(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32337365
GeneBRCA2
is asnp
is mentioned by
dbSNPrs730881604
ebirs730881604
HLIrs730881604
Exacrs730881604
Varsomers730881604
Maprs730881604
PheGenIrs730881604
hapmaprs730881604
1000 genomesrs730881604
hgdprs730881604
ensemblrs730881604
gopubmedrs730881604
geneviewrs730881604
scholarrs730881604
googlers730881604
pharmgkbrs730881604
gwascentralrs730881604
openSNPrs730881604
23andMers730881604
23andMe allrs730881604
SNP Nexus

SNPshotrs730881604
SNPdbers730881604
MSV3drs730881604
GWAS Ctlgrs730881604
Max Magnitude0
ClinVar
Risk rs730881604(;)
Alt rs730881604(;)
Reference rs730881604(A;A)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911502delA
CLNSRC
CLNACC RCV000160279.1,