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rs397508014

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508014(-;-)
Make rs397508014(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379404
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508014
ebirs397508014
HLIrs397508014
Exacrs397508014
Varsomers397508014
Maprs397508014
PheGenIrs397508014
hapmaprs397508014
1000 genomesrs397508014
hgdprs397508014
ensemblrs397508014
gopubmedrs397508014
geneviewrs397508014
scholarrs397508014
googlers397508014
pharmgkbrs397508014
gwascentralrs397508014
openSNPrs397508014
23andMers397508014
23andMe allrs397508014
SNP Nexus

SNPshotrs397508014
SNPdbers397508014
MSV3drs397508014
GWAS Ctlgrs397508014
Max Magnitude0
ClinVar
Risk rs397508014(;)
Alt rs397508014(;)
Reference rs397508014(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.32953541delA
CLNSRC ClinVar
CLNACC RCV000045639.2,