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

rs397508887

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTCCTGA;CTCCTGA) 0 common in clinvar
Make rs397508887(-;-)
Make rs397508887(-;CTCCTGA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093942
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508887
ebirs397508887
HLIrs397508887
Exacrs397508887
Varsomers397508887
Maprs397508887
PheGenIrs397508887
hapmaprs397508887
1000 genomesrs397508887
hgdprs397508887
ensemblrs397508887
gopubmedrs397508887
geneviewrs397508887
scholarrs397508887
googlers397508887
pharmgkbrs397508887
gwascentralrs397508887
openSNPrs397508887
23andMers397508887
23andMe allrs397508887
SNP Nexus

SNPshotrs397508887
SNPdbers397508887
MSV3drs397508887
GWAS Ctlgrs397508887
Max Magnitude0
ClinVar
Risk rs397508887(;)
Alt rs397508887(;)
Reference rs397508887(CTCCTGA;CTCCTGA)
Significance Pathogenic
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.41245959_41245965delTCAGGAG
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000047533.2, RCV000111651.1,