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rs730881601

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;GATA) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs730881601(GATA;GATA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32329484
GeneBRCA2
is asnp
is mentioned by
dbSNPrs730881601
dbSNP (old)rs730881601
ClinGenrs730881601
ebirs730881601
HLIrs730881601
Exacrs730881601
Gnomadrs730881601
Varsomers730881601
Maprs730881601
PheGenIrs730881601
Biobankrs730881601
1000 genomesrs730881601
hgdprs730881601
ensemblrs730881601
gopubmedrs730881601
geneviewrs730881601
scholarrs730881601
googlers730881601
pharmgkbrs730881601
gwascentralrs730881601
openSNPrs730881601
23andMers730881601
23andMe allrs730881601
SNP Nexus

SNPshotrs730881601
SNPdbers730881601
MSV3drs730881601
GWAS Ctlgrs730881601
Max Magnitude6
ClinVar
Risk rs730881601(GATA;GATA)
Alt rs730881601(GATA;GATA)
Reference Rs730881601(-;-)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer not provided
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 not provided
Reversed 0
HGVS NC_000013.10:g.32903618_32903621dupGATA
CLNSRC
CLNACC RCV000160264.1, RCV000241290.1, RCV000486203.1,