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rs397507976

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AATCTCTTATGTTA;AATCTCTTATGTTA) 0 common in clinvar
(TCTCTTATGTTAAA;TCTCTTATGTTAAA) 0 common in clinvar
Make rs397507976(-;-)
Make rs397507976(-;TCTCTTATGTTAAA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363519
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507976
ebirs397507976
HLIrs397507976
Exacrs397507976
Varsomers397507976
Maprs397507976
PheGenIrs397507976
hapmaprs397507976
1000 genomesrs397507976
hgdprs397507976
ensemblrs397507976
gopubmedrs397507976
geneviewrs397507976
scholarrs397507976
googlers397507976
pharmgkbrs397507976
gwascentralrs397507976
openSNPrs397507976
23andMers397507976
23andMe allrs397507976
SNP Nexus

SNPshotrs397507976
SNPdbers397507976
MSV3drs397507976
GWAS Ctlgrs397507976
Max Magnitude0
ClinVar
Risk rs397507976(;)
Alt rs397507976(;)
Reference rs397507976(AATCTCTTATGTTA;AATCTCTTATGTTA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32937656_32937669delTCTCTTATGTTAAA
CLNSRC ClinVar
CLNACC RCV000045470.2,