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rs397507746

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs397507746(-;-)
Make rs397507746(-;AA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339203
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507746
ebirs397507746
HLIrs397507746
Exacrs397507746
Varsomers397507746
Maprs397507746
PheGenIrs397507746
hapmaprs397507746
1000 genomesrs397507746
hgdprs397507746
ensemblrs397507746
gopubmedrs397507746
geneviewrs397507746
scholarrs397507746
googlers397507746
pharmgkbrs397507746
gwascentralrs397507746
openSNPrs397507746
23andMers397507746
23andMe allrs397507746
SNP Nexus

SNPshotrs397507746
SNPdbers397507746
MSV3drs397507746
GWAS Ctlgrs397507746
Max Magnitude0
ClinVar
Risk rs397507746(;)
Alt rs397507746(;)
Reference rs397507746(AA;AA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913340_32913341delAA
CLNSRC ClinVar
CLNACC RCV000044505.2,