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rs397507695

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507695(-;-)
Make rs397507695(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338242
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507695
ebirs397507695
HLIrs397507695
Exacrs397507695
Varsomers397507695
Maprs397507695
PheGenIrs397507695
hapmaprs397507695
1000 genomesrs397507695
hgdprs397507695
ensemblrs397507695
gopubmedrs397507695
geneviewrs397507695
scholarrs397507695
googlers397507695
pharmgkbrs397507695
gwascentralrs397507695
openSNPrs397507695
23andMers397507695
23andMe allrs397507695
SNP Nexus

SNPshotrs397507695
SNPdbers397507695
MSV3drs397507695
GWAS Ctlgrs397507695
Max Magnitude0
ClinVar
Risk rs397507695(;)
Alt rs397507695(;)
Reference rs397507695(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.32912379delA
CLNSRC ClinVar
CLNACC RCV000044297.2,