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rs397507895

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs397507895(-;ATTTGTATGAACATCTGAC)
Make rs397507895(ATTTGTATGAACATCTGAC;ATTTGTATGAACATCTGAC)
ReferenceGRCh38 38.1/141
Chromosome13
Position32354953
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507895
dbSNP (old)rs397507895
ClinGenrs397507895
ebirs397507895
HLIrs397507895
Exacrs397507895
Gnomadrs397507895
Varsomers397507895
Maprs397507895
PheGenIrs397507895
Biobankrs397507895
1000 genomesrs397507895
hgdprs397507895
ensemblrs397507895
gopubmedrs397507895
geneviewrs397507895
scholarrs397507895
googlers397507895
pharmgkbrs397507895
gwascentralrs397507895
openSNPrs397507895
23andMers397507895
23andMe allrs397507895
SNP Nexus

SNPshotrs397507895
SNPdbers397507895
MSV3drs397507895
GWAS Ctlgrs397507895
Max Magnitude0
ClinVar
Risk rs397507895(CATTTGTATGAACATCTGA;CATTTGTATGAACATCTGA)
Alt rs397507895(CATTTGTATGAACATCTGA;CATTTGTATGAACATCTGA)
Reference Rs397507895(-;-)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32929072_32929090dup19
CLNSRC ClinVar
CLNACC RCV000045138.2,