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rs397507711

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507711(-;-)
Make rs397507711(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338526
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507711
ebirs397507711
HLIrs397507711
Exacrs397507711
Varsomers397507711
Maprs397507711
PheGenIrs397507711
hapmaprs397507711
1000 genomesrs397507711
hgdprs397507711
ensemblrs397507711
gopubmedrs397507711
geneviewrs397507711
scholarrs397507711
googlers397507711
pharmgkbrs397507711
gwascentralrs397507711
openSNPrs397507711
23andMers397507711
23andMe allrs397507711
SNP Nexus

SNPshotrs397507711
SNPdbers397507711
MSV3drs397507711
GWAS Ctlgrs397507711
Max Magnitude0
ClinVar
Risk rs397507711(;)
Alt rs397507711(;)
Reference rs397507711(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32912663delG
CLNSRC ClinVar
CLNACC RCV000044366.2,