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rs397507858

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507858(-;-)
Make rs397507858(-;TA)
Make rs397507858(TA;TA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340803
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507858
ebirs397507858
HLIrs397507858
Exacrs397507858
Varsomers397507858
Maprs397507858
PheGenIrs397507858
hapmaprs397507858
1000 genomesrs397507858
hgdprs397507858
ensemblrs397507858
gopubmedrs397507858
geneviewrs397507858
scholarrs397507858
googlers397507858
pharmgkbrs397507858
gwascentralrs397507858
openSNPrs397507858
23andMers397507858
23andMe allrs397507858
SNP Nexus

SNPshotrs397507858
SNPdbers397507858
MSV3drs397507858
GWAS Ctlgrs397507858
Max Magnitude0
ClinVar
Risk rs397507858(TA;TA)
Alt rs397507858(TA;TA)
Reference rs397507858(;)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914939_32914940dupTA
CLNSRC ClinVar
CLNACC RCV000044957.2, RCV000165176.1, RCV000238618.1,