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rs397507863

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGTTG;AGTTG) 0 common in clinvar
Make rs397507863(-;-)
Make rs397507863(-;AGTTG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340846
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507863
ebirs397507863
HLIrs397507863
Exacrs397507863
Varsomers397507863
Maprs397507863
PheGenIrs397507863
hapmaprs397507863
1000 genomesrs397507863
hgdprs397507863
ensemblrs397507863
gopubmedrs397507863
geneviewrs397507863
scholarrs397507863
googlers397507863
pharmgkbrs397507863
gwascentralrs397507863
openSNPrs397507863
23andMers397507863
23andMe allrs397507863
SNP Nexus

SNPshotrs397507863
SNPdbers397507863
MSV3drs397507863
GWAS Ctlgrs397507863
Max Magnitude0
ClinVar
Risk rs397507863(;)
Alt rs397507863(;)
Reference rs397507863(AGTTG;AGTTG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914983_32914987delAGTTG
CLNSRC ClinVar
CLNACC RCV000044972.2,