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rs397507668

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507668(-;-)
Make rs397507668(-;AG)
Make rs397507668(AG;AG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337804
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507668
ebirs397507668
HLIrs397507668
Exacrs397507668
Varsomers397507668
Maprs397507668
PheGenIrs397507668
hapmaprs397507668
1000 genomesrs397507668
hgdprs397507668
ensemblrs397507668
gopubmedrs397507668
geneviewrs397507668
scholarrs397507668
googlers397507668
pharmgkbrs397507668
gwascentralrs397507668
openSNPrs397507668
23andMers397507668
23andMe allrs397507668
SNP Nexus

SNPshotrs397507668
SNPdbers397507668
MSV3drs397507668
GWAS Ctlgrs397507668
Max Magnitude0
ClinVar
Risk rs397507668(AG;AG)
Alt rs397507668(AG;AG)
Reference rs397507668(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911941_32911942insAG
CLNSRC ClinVar
CLNACC RCV000044196.2,