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rs397508035

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAAA;AAAA) 0 common in clinvar
Make rs397508035(-;-)
Make rs397508035(-;AAAA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379890
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508035
ebirs397508035
HLIrs397508035
Exacrs397508035
Varsomers397508035
Maprs397508035
PheGenIrs397508035
hapmaprs397508035
1000 genomesrs397508035
hgdprs397508035
ensemblrs397508035
gopubmedrs397508035
geneviewrs397508035
scholarrs397508035
googlers397508035
pharmgkbrs397508035
gwascentralrs397508035
openSNPrs397508035
23andMers397508035
23andMe allrs397508035
SNP Nexus

SNPshotrs397508035
SNPdbers397508035
MSV3drs397508035
GWAS Ctlgrs397508035
Max Magnitude0
ClinVar
Risk rs397508035(;)
Alt rs397508035(;)
Reference rs397508035(AAAA;AAAA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32954027_32954030delAAAA
CLNSRC ClinVar
CLNACC RCV000045709.2,