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rs397507955

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs397507955(-;-)
Make rs397507955(-;GA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363231
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507955
ebirs397507955
HLIrs397507955
Exacrs397507955
Varsomers397507955
Maprs397507955
PheGenIrs397507955
hapmaprs397507955
1000 genomesrs397507955
hgdprs397507955
ensemblrs397507955
gopubmedrs397507955
geneviewrs397507955
scholarrs397507955
googlers397507955
pharmgkbrs397507955
gwascentralrs397507955
openSNPrs397507955
23andMers397507955
23andMe allrs397507955
SNP Nexus

SNPshotrs397507955
SNPdbers397507955
MSV3drs397507955
GWAS Ctlgrs397507955
Max Magnitude0
ClinVar
Risk rs397507955(;)
Alt rs397507955(;)
Reference rs397507955(GA;GA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32937368_32937369delGA
CLNSRC ClinVar
CLNACC RCV000045392.2,