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rs397507333

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGA;AAGA) 0 common in clinvar
(AGAA;AGAA) 0 common in clinvar
Make rs397507333(-;-)
Make rs397507333(-;AGAA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338770
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507333
ebirs397507333
HLIrs397507333
Exacrs397507333
Varsomers397507333
Maprs397507333
PheGenIrs397507333
hapmaprs397507333
1000 genomesrs397507333
hgdprs397507333
ensemblrs397507333
gopubmedrs397507333
geneviewrs397507333
scholarrs397507333
googlers397507333
pharmgkbrs397507333
gwascentralrs397507333
openSNPrs397507333
23andMers397507333
23andMe allrs397507333
SNP Nexus

SNPshotrs397507333
SNPdbers397507333
MSV3drs397507333
GWAS Ctlgrs397507333
Max Magnitude0
ClinVar
Risk rs397507333(;)
Alt rs397507333(;)
Reference rs397507333(AAGA;AAGA)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome not provided
Reversed 0
HGVS NC_000013.10:g.32912907_32912910delAGAA
CLNSRC ClinVar
CLNACC RCV000031483.4, RCV000044410.3, RCV000213169.1,