Have questions? Visit https://www.reddit.com/r/SNPedia

rs397508026

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATCATCAGATTTAT;ATCATCAGATTTAT) 0 common in clinvar
(CATCAGATTTATAT;CATCAGATTTATAT) 0 common in clinvar
Make rs397508026(-;-)
Make rs397508026(-;CATCAGATTTATAT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379774
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508026
ebirs397508026
HLIrs397508026
Exacrs397508026
Varsomers397508026
Maprs397508026
PheGenIrs397508026
hapmaprs397508026
1000 genomesrs397508026
hgdprs397508026
ensemblrs397508026
gopubmedrs397508026
geneviewrs397508026
scholarrs397508026
googlers397508026
pharmgkbrs397508026
gwascentralrs397508026
openSNPrs397508026
23andMers397508026
23andMe allrs397508026
SNP Nexus

SNPshotrs397508026
SNPdbers397508026
MSV3drs397508026
GWAS Ctlgrs397508026
Max Magnitude0
ClinVar
Risk rs397508026(;)
Alt rs397508026(;)
Reference rs397508026(ATCATCAGATTTAT;ATCATCAGATTTAT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32953911_32953924delCATCAGATTTATAT
CLNSRC ClinVar
CLNACC RCV000045678.2,