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rs397507687

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAAATTTT;GAAATTTT) 0 common in clinvar
(TTTTGAAA;TTTTGAAA) 0 common in clinvar
Make rs397507687(-;-)
Make rs397507687(-;GAAATTTT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32316497
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507687
ebirs397507687
HLIrs397507687
Exacrs397507687
Varsomers397507687
Maprs397507687
PheGenIrs397507687
hapmaprs397507687
1000 genomesrs397507687
hgdprs397507687
ensemblrs397507687
gopubmedrs397507687
geneviewrs397507687
scholarrs397507687
googlers397507687
pharmgkbrs397507687
gwascentralrs397507687
openSNPrs397507687
23andMers397507687
23andMe allrs397507687
SNP Nexus

SNPshotrs397507687
SNPdbers397507687
MSV3drs397507687
GWAS Ctlgrs397507687
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397507687(TTTTGAAA;TTTTGAAA)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32890634_32890641delGAAATTTT
CLNSRC ClinVar
CLNACC RCV000044269.2, RCV000256827.2,