Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507862

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGTT;AGTT) 0 common in clinvar
Make rs397507862(-;-)
Make rs397507862(-;AGTT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340846
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507862
ebirs397507862
HLIrs397507862
Exacrs397507862
Varsomers397507862
Maprs397507862
PheGenIrs397507862
hapmaprs397507862
1000 genomesrs397507862
hgdprs397507862
ensemblrs397507862
gopubmedrs397507862
geneviewrs397507862
scholarrs397507862
googlers397507862
pharmgkbrs397507862
gwascentralrs397507862
openSNPrs397507862
23andMers397507862
23andMe allrs397507862
SNP Nexus

SNPshotrs397507862
SNPdbers397507862
MSV3drs397507862
GWAS Ctlgrs397507862
Max Magnitude0
ClinVar
Risk rs397507862(;)
Alt rs397507862(;)
Reference rs397507862(AGTT;AGTT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914983_32914986delAGTT
CLNSRC ClinVar
CLNACC RCV000044971.2,