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rs397507810

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507810(-;-)
Make rs397507810(-;AGTT)
Make rs397507810(AGTT;AGTT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340209
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507810
ebirs397507810
HLIrs397507810
Exacrs397507810
Varsomers397507810
Maprs397507810
PheGenIrs397507810
hapmaprs397507810
1000 genomesrs397507810
hgdprs397507810
ensemblrs397507810
gopubmedrs397507810
geneviewrs397507810
scholarrs397507810
googlers397507810
pharmgkbrs397507810
gwascentralrs397507810
openSNPrs397507810
23andMers397507810
23andMe allrs397507810
SNP Nexus

SNPshotrs397507810
SNPdbers397507810
MSV3drs397507810
GWAS Ctlgrs397507810
Max Magnitude0
ClinVar
Risk rs397507810(GTTA;GTTA)
Alt rs397507810(GTTA;GTTA)
Reference rs397507810(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914343_32914346dupAGTT
CLNSRC ClinVar
CLNACC RCV000044774.2,