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rs397507693

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507693(-;-)
Make rs397507693(-;A)
Make rs397507693(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338218
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507693
ebirs397507693
HLIrs397507693
Exacrs397507693
Varsomers397507693
Maprs397507693
PheGenIrs397507693
hapmaprs397507693
1000 genomesrs397507693
hgdprs397507693
ensemblrs397507693
gopubmedrs397507693
geneviewrs397507693
scholarrs397507693
googlers397507693
pharmgkbrs397507693
gwascentralrs397507693
openSNPrs397507693
23andMers397507693
23andMe allrs397507693
SNP Nexus

SNPshotrs397507693
SNPdbers397507693
MSV3drs397507693
GWAS Ctlgrs397507693
Max Magnitude0
ClinVar
Risk rs397507693(A;A)
Alt rs397507693(A;A)
Reference rs397507693(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32912355dupA
CLNSRC ClinVar
CLNACC RCV000044291.2,