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rs397507830

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507830(-;-)
Make rs397507830(-;CTTA)
Make rs397507830(CTTA;CTTA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326595
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507830
ebirs397507830
HLIrs397507830
Exacrs397507830
Varsomers397507830
Maprs397507830
PheGenIrs397507830
hapmaprs397507830
1000 genomesrs397507830
hgdprs397507830
ensemblrs397507830
gopubmedrs397507830
geneviewrs397507830
scholarrs397507830
googlers397507830
pharmgkbrs397507830
gwascentralrs397507830
openSNPrs397507830
23andMers397507830
23andMe allrs397507830
SNP Nexus

SNPshotrs397507830
SNPdbers397507830
MSV3drs397507830
GWAS Ctlgrs397507830
Max Magnitude0
ClinVar
Risk rs397507830(CTTA;CTTA)
Alt rs397507830(CTTA;CTTA)
Reference rs397507830(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32900729_32900732dupCTTA
CLNSRC ClinVar
CLNACC RCV000044847.2,