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rs397507383

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTTGAT;CTTGAT) 0 common in clinvar
Make rs397507383(AG;AG)
Make rs397507383(AG;CTTGAT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355038
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507383
ebirs397507383
HLIrs397507383
Exacrs397507383
Varsomers397507383
Maprs397507383
PheGenIrs397507383
hapmaprs397507383
1000 genomesrs397507383
hgdprs397507383
ensemblrs397507383
gopubmedrs397507383
geneviewrs397507383
scholarrs397507383
googlers397507383
pharmgkbrs397507383
gwascentralrs397507383
openSNPrs397507383
23andMers397507383
23andMe allrs397507383
SNP Nexus

SNPshotrs397507383
SNPdbers397507383
MSV3drs397507383
GWAS Ctlgrs397507383
Max Magnitude0
ClinVar
Risk rs397507383(AG;AG)
Alt rs397507383(AG;AG)
Reference rs397507383(CTTGAT;CTTGAT)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32929175_32929180delCTTGATinsAG
CLNSRC ClinVar
CLNACC RCV000031669.3,