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rs397507911

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507911(-;-)
Make rs397507911(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355175
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507911
ebirs397507911
HLIrs397507911
Exacrs397507911
Varsomers397507911
Maprs397507911
PheGenIrs397507911
hapmaprs397507911
1000 genomesrs397507911
hgdprs397507911
ensemblrs397507911
gopubmedrs397507911
geneviewrs397507911
scholarrs397507911
googlers397507911
pharmgkbrs397507911
gwascentralrs397507911
openSNPrs397507911
23andMers397507911
23andMe allrs397507911
SNP Nexus

SNPshotrs397507911
SNPdbers397507911
MSV3drs397507911
GWAS Ctlgrs397507911
Max Magnitude0
ClinVar
Risk rs397507911(;)
Alt rs397507911(;)
Reference rs397507911(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.32929312delG
CLNSRC ClinVar
CLNACC RCV000045189.2,