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rs397507723

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507723(-;-)
Make rs397507723(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338890
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507723
ebirs397507723
HLIrs397507723
Exacrs397507723
Varsomers397507723
Maprs397507723
PheGenIrs397507723
hapmaprs397507723
1000 genomesrs397507723
hgdprs397507723
ensemblrs397507723
gopubmedrs397507723
geneviewrs397507723
scholarrs397507723
googlers397507723
pharmgkbrs397507723
gwascentralrs397507723
openSNPrs397507723
23andMers397507723
23andMe allrs397507723
SNP Nexus

SNPshotrs397507723
SNPdbers397507723
MSV3drs397507723
GWAS Ctlgrs397507723
Max Magnitude0
ClinVar
Risk rs397507723(;)
Alt rs397507723(;)
Reference rs397507723(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.32913027delG
CLNSRC ClinVar
CLNACC RCV000044430.2,