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rs397507697

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAC;GAC) 0 common in clinvar
Make rs397507697(-;-)
Make rs397507697(-;GAC)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338255
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507697
ebirs397507697
HLIrs397507697
Exacrs397507697
Varsomers397507697
Maprs397507697
PheGenIrs397507697
hapmaprs397507697
1000 genomesrs397507697
hgdprs397507697
ensemblrs397507697
gopubmedrs397507697
geneviewrs397507697
scholarrs397507697
googlers397507697
pharmgkbrs397507697
gwascentralrs397507697
openSNPrs397507697
23andMers397507697
23andMe allrs397507697
SNP Nexus

SNPshotrs397507697
SNPdbers397507697
MSV3drs397507697
GWAS Ctlgrs397507697
Max Magnitude0
ClinVar
Risk rs397507697(;)
Alt rs397507697(;)
Reference rs397507697(GAC;GAC)
Significance Untested
Disease Hereditary breast and ovarian cancer syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32912392_32912394delGAC
CLNSRC ClinVar
CLNACC RCV000044300.3, RCV000218170.1,