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rs397507956

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507956(-;-)
Make rs397507956(-;AG)
Make rs397507956(AG;AG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363235
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507956
ebirs397507956
HLIrs397507956
Exacrs397507956
Varsomers397507956
Maprs397507956
PheGenIrs397507956
hapmaprs397507956
1000 genomesrs397507956
hgdprs397507956
ensemblrs397507956
gopubmedrs397507956
geneviewrs397507956
scholarrs397507956
googlers397507956
pharmgkbrs397507956
gwascentralrs397507956
openSNPrs397507956
23andMers397507956
23andMe allrs397507956
SNP Nexus

SNPshotrs397507956
SNPdbers397507956
MSV3drs397507956
GWAS Ctlgrs397507956
Max Magnitude0
ClinVar
Risk rs397507956(AG;AG)
Alt rs397507956(AG;AG)
Reference rs397507956(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32937371_32937372dupAG
CLNSRC ClinVar
CLNACC RCV000045395.2,