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rs273897657

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs273897657(-;-)
Make rs273897657(-;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43115724
GeneBRCA1
is asnp
is mentioned by
dbSNPrs273897657
ebirs273897657
HLIrs273897657
Exacrs273897657
Varsomers273897657
Maprs273897657
PheGenIrs273897657
hapmaprs273897657
1000 genomesrs273897657
hgdprs273897657
ensemblrs273897657
gopubmedrs273897657
geneviewrs273897657
scholarrs273897657
googlers273897657
pharmgkbrs273897657
gwascentralrs273897657
openSNPrs273897657
23andMers273897657
23andMe allrs273897657
SNP Nexus

SNPshotrs273897657
SNPdbers273897657
MSV3drs273897657
GWAS Ctlgrs273897657
Max Magnitude0
ClinVar
Risk rs273897657(;)
Alt rs273897657(;)
Reference rs273897657(T;T)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41267741delA
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000047429.2, RCV000111850.1,