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rs397507743

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507743(-;-)
Make rs397507743(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339163
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507743
ebirs397507743
HLIrs397507743
Exacrs397507743
Varsomers397507743
Maprs397507743
PheGenIrs397507743
hapmaprs397507743
1000 genomesrs397507743
hgdprs397507743
ensemblrs397507743
gopubmedrs397507743
geneviewrs397507743
scholarrs397507743
googlers397507743
pharmgkbrs397507743
gwascentralrs397507743
openSNPrs397507743
23andMers397507743
23andMe allrs397507743
SNP Nexus

SNPshotrs397507743
SNPdbers397507743
MSV3drs397507743
GWAS Ctlgrs397507743
Max Magnitude0
ClinVar
Risk rs397507743(;)
Alt rs397507743(;)
Reference rs397507743(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.32913300delA
CLNSRC ClinVar
CLNACC RCV000044496.2,