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rs397507905

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACCT;ACCT) 0 common in clinvar
Make rs397507905(-;-)
Make rs397507905(-;ACCT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355077
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507905
ebirs397507905
HLIrs397507905
Exacrs397507905
Varsomers397507905
Maprs397507905
PheGenIrs397507905
hapmaprs397507905
1000 genomesrs397507905
hgdprs397507905
ensemblrs397507905
gopubmedrs397507905
geneviewrs397507905
scholarrs397507905
googlers397507905
pharmgkbrs397507905
gwascentralrs397507905
openSNPrs397507905
23andMers397507905
23andMe allrs397507905
SNP Nexus

SNPshotrs397507905
SNPdbers397507905
MSV3drs397507905
GWAS Ctlgrs397507905
Max Magnitude0
ClinVar
Risk rs397507905(;)
Alt rs397507905(;)
Reference rs397507905(ACCT;ACCT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32929214_32929217delACCT
CLNSRC ClinVar
CLNACC RCV000045169.2,