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rs273902778

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs273902778(-;-)
Make rs273902778(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43124036
GeneBRCA1, NBR2
is asnp
is mentioned by
dbSNPrs273902778
ebirs273902778
HLIrs273902778
Exacrs273902778
Varsomers273902778
Maprs273902778
PheGenIrs273902778
hapmaprs273902778
1000 genomesrs273902778
hgdprs273902778
ensemblrs273902778
gopubmedrs273902778
geneviewrs273902778
scholarrs273902778
googlers273902778
pharmgkbrs273902778
gwascentralrs273902778
openSNPrs273902778
23andMers273902778
23andMe allrs273902778
SNP Nexus

SNPshotrs273902778
SNPdbers273902778
MSV3drs273902778
GWAS Ctlgrs273902778
Max Magnitude0
ClinVar
Risk rs273902778(;)
Alt rs273902778(;)
Reference rs273902778(A;A)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene NBR2 BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41276053delT
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000049073.2, RCV000111664.1,