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rs397507769

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507769(-;-)
Make rs397507769(-;A)
Make rs397507769(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339535
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507769
ebirs397507769
HLIrs397507769
Exacrs397507769
Varsomers397507769
Maprs397507769
PheGenIrs397507769
hapmaprs397507769
1000 genomesrs397507769
hgdprs397507769
ensemblrs397507769
gopubmedrs397507769
geneviewrs397507769
scholarrs397507769
googlers397507769
pharmgkbrs397507769
gwascentralrs397507769
openSNPrs397507769
23andMers397507769
23andMe allrs397507769
SNP Nexus

SNPshotrs397507769
SNPdbers397507769
MSV3drs397507769
GWAS Ctlgrs397507769
Max Magnitude0
ClinVar
Risk rs397507769(A;A)
Alt rs397507769(A;A)
Reference rs397507769(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913672dupA
CLNSRC ClinVar
CLNACC RCV000044595.2,