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rs397507927

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TCTAAACATT;TCTAAACATT) 0 common in clinvar
(TTTCTAAACA;TTTCTAAACA) 0 common in clinvar
Make rs397507927(-;-)
Make rs397507927(-;TCTAAACATT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32357760
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507927
ebirs397507927
HLIrs397507927
Exacrs397507927
Varsomers397507927
Maprs397507927
PheGenIrs397507927
hapmaprs397507927
1000 genomesrs397507927
hgdprs397507927
ensemblrs397507927
gopubmedrs397507927
geneviewrs397507927
scholarrs397507927
googlers397507927
pharmgkbrs397507927
gwascentralrs397507927
openSNPrs397507927
23andMers397507927
23andMe allrs397507927
SNP Nexus

SNPshotrs397507927
SNPdbers397507927
MSV3drs397507927
GWAS Ctlgrs397507927
Max Magnitude0
ClinVar
Risk rs397507927(;)
Alt rs397507927(;)
Reference rs397507927(TTTCTAAACA;TTTCTAAACA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32931897_32931906delTCTAAACATT
CLNSRC ClinVar
CLNACC RCV000045273.2,