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rs397507929

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507929(-;-)
Make rs397507929(-;AAAC)
Make rs397507929(AAAC;AAAC)
ReferenceGRCh38 38.1/141
Chromosome13
Position32357799
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507929
ebirs397507929
HLIrs397507929
Exacrs397507929
Varsomers397507929
Maprs397507929
PheGenIrs397507929
hapmaprs397507929
1000 genomesrs397507929
hgdprs397507929
ensemblrs397507929
gopubmedrs397507929
geneviewrs397507929
scholarrs397507929
googlers397507929
pharmgkbrs397507929
gwascentralrs397507929
openSNPrs397507929
23andMers397507929
23andMe allrs397507929
SNP Nexus

SNPshotrs397507929
SNPdbers397507929
MSV3drs397507929
GWAS Ctlgrs397507929
Max Magnitude0
ClinVar
Risk rs397507929(AAAC;AAAC)
Alt rs397507929(AAAC;AAAC)
Reference rs397507929(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32931936_32931937insAAAC
CLNSRC ClinVar
CLNACC RCV000045280.2,