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rs397507775

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTAAGT;TTAAGT) 0 common in clinvar
(TTTAAG;TTTAAG) 0 common in clinvar
Make rs397507775(-;-)
Make rs397507775(-;TTAAGT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339573
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507775
ebirs397507775
HLIrs397507775
Exacrs397507775
Varsomers397507775
Maprs397507775
PheGenIrs397507775
hapmaprs397507775
1000 genomesrs397507775
hgdprs397507775
ensemblrs397507775
gopubmedrs397507775
geneviewrs397507775
scholarrs397507775
googlers397507775
pharmgkbrs397507775
gwascentralrs397507775
openSNPrs397507775
23andMers397507775
23andMe allrs397507775
SNP Nexus

SNPshotrs397507775
SNPdbers397507775
MSV3drs397507775
GWAS Ctlgrs397507775
Max Magnitude0
ClinVar
Risk rs397507775(;)
Alt rs397507775(;)
Reference rs397507775(TTTAAG;TTTAAG)
Significance Untested
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32913710_32913715delTTAAGT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044615.3, RCV000113403.1, RCV000129461.2,