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rs397508029

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508029(G;T)
Make rs397508029(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379803
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508029
ebirs397508029
HLIrs397508029
Exacrs397508029
Varsomers397508029
Maprs397508029
PheGenIrs397508029
hapmaprs397508029
1000 genomesrs397508029
hgdprs397508029
ensemblrs397508029
gopubmedrs397508029
geneviewrs397508029
scholarrs397508029
googlers397508029
pharmgkbrs397508029
gwascentralrs397508029
openSNPrs397508029
23andMers397508029
23andMe allrs397508029
SNP Nexus

SNPshotrs397508029
SNPdbers397508029
MSV3drs397508029
GWAS Ctlgrs397508029
Max Magnitude0
ClinVar
Risk rs397508029(T;T)
Alt rs397508029(T;T)
Reference rs397508029(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32953940G>T
CLNSRC ClinVar
CLNACC RCV000045687.2,