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rs397508001

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AACC;AACC) 0 common in clinvar
(ACCA;ACCA) 0 common in clinvar
Make rs397508001(-;-)
Make rs397508001(-;ACCA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376683
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508001
ebirs397508001
HLIrs397508001
Exacrs397508001
Varsomers397508001
Maprs397508001
PheGenIrs397508001
hapmaprs397508001
1000 genomesrs397508001
hgdprs397508001
ensemblrs397508001
gopubmedrs397508001
geneviewrs397508001
scholarrs397508001
googlers397508001
pharmgkbrs397508001
gwascentralrs397508001
openSNPrs397508001
23andMers397508001
23andMe allrs397508001
SNP Nexus

SNPshotrs397508001
SNPdbers397508001
MSV3drs397508001
GWAS Ctlgrs397508001
Max Magnitude0
ClinVar
Risk rs397508001(;)
Alt rs397508001(;)
Reference rs397508001(AACC;AACC)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32950820_32950823delACCA
CLNSRC ClinVar
CLNACC RCV000045589.2,