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rs397508021

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508021(-;-)
Make rs397508021(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379508
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508021
ebirs397508021
HLIrs397508021
Exacrs397508021
Varsomers397508021
Maprs397508021
PheGenIrs397508021
hapmaprs397508021
1000 genomesrs397508021
hgdprs397508021
ensemblrs397508021
gopubmedrs397508021
geneviewrs397508021
scholarrs397508021
googlers397508021
pharmgkbrs397508021
gwascentralrs397508021
openSNPrs397508021
23andMers397508021
23andMe allrs397508021
SNP Nexus

SNPshotrs397508021
SNPdbers397508021
MSV3drs397508021
GWAS Ctlgrs397508021
Max Magnitude0
ClinVar
Risk rs397508021(;)
Alt rs397508021(;)
Reference rs397508021(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32953645delA
CLNSRC ClinVar
CLNACC RCV000045663.2,