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rs397507818

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507818(-;-)
Make rs397507818(-;A)
Make rs397507818(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340339
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507818
ebirs397507818
HLIrs397507818
Exacrs397507818
Varsomers397507818
Maprs397507818
PheGenIrs397507818
hapmaprs397507818
1000 genomesrs397507818
hgdprs397507818
ensemblrs397507818
gopubmedrs397507818
geneviewrs397507818
scholarrs397507818
googlers397507818
pharmgkbrs397507818
gwascentralrs397507818
openSNPrs397507818
23andMers397507818
23andMe allrs397507818
SNP Nexus

SNPshotrs397507818
SNPdbers397507818
MSV3drs397507818
GWAS Ctlgrs397507818
Max Magnitude0
ClinVar
Risk rs397507818(A;A)
Alt rs397507818(A;A)
Reference rs397507818(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914476dupA
CLNSRC ClinVar
CLNACC RCV000044812.2,