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rs397507705

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507705(-;-)
Make rs397507705(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338456
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507705
ebirs397507705
HLIrs397507705
Exacrs397507705
Varsomers397507705
Maprs397507705
PheGenIrs397507705
hapmaprs397507705
1000 genomesrs397507705
hgdprs397507705
ensemblrs397507705
gopubmedrs397507705
geneviewrs397507705
scholarrs397507705
googlers397507705
pharmgkbrs397507705
gwascentralrs397507705
openSNPrs397507705
23andMers397507705
23andMe allrs397507705
SNP Nexus

SNPshotrs397507705
SNPdbers397507705
MSV3drs397507705
GWAS Ctlgrs397507705
Max Magnitude0
ClinVar
Risk rs397507705(;)
Alt rs397507705(;)
Reference rs397507705(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.32912593delA
CLNSRC ClinVar
CLNACC RCV000044350.2,