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rs397507809

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507809(-;-)
Make rs397507809(-;ATCACCTTG)
Make rs397507809(ATCACCTTG;ATCACCTTG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340198
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507809
ebirs397507809
HLIrs397507809
Exacrs397507809
Varsomers397507809
Maprs397507809
PheGenIrs397507809
hapmaprs397507809
1000 genomesrs397507809
hgdprs397507809
ensemblrs397507809
gopubmedrs397507809
geneviewrs397507809
scholarrs397507809
googlers397507809
pharmgkbrs397507809
gwascentralrs397507809
openSNPrs397507809
23andMers397507809
23andMe allrs397507809
SNP Nexus

SNPshotrs397507809
SNPdbers397507809
MSV3drs397507809
GWAS Ctlgrs397507809
Max Magnitude0
ClinVar
Risk rs397507809(ATCACCTTG;ATCACCTTG)
Alt rs397507809(ATCACCTTG;ATCACCTTG)
Reference rs397507809(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914327_32914335dupATCACCTTG
CLNSRC ClinVar
CLNACC RCV000044769.2,