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rs397508861

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;A) 6 BRCA1 variant considered pathogenic for breast cancer
(A;A) 0 common in clinvar


Make rs397508861(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094160
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508861
dbSNP (old)rs397508861
ClinGenrs397508861
ebirs397508861
HLIrs397508861
Exacrs397508861
Varsomers397508861
Maprs397508861
PheGenIrs397508861
Biobankrs397508861
1000 genomesrs397508861
hgdprs397508861
ensemblrs397508861
gopubmedrs397508861
geneviewrs397508861
scholarrs397508861
googlers397508861
pharmgkbrs397508861
gwascentralrs397508861
openSNPrs397508861
23andMers397508861
23andMe allrs397508861
SNP Nexus

SNPshotrs397508861
SNPdbers397508861
MSV3drs397508861
GWAS Ctlgrs397508861
Max Magnitude6
ClinVar
Risk rs397508861(-;-)
Alt rs397508861(-;-)
Reference Rs397508861(A;A)
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.41246177delT
CLNSRC ClinVar
CLNACC RCV000047444.2, RCV000256751.2,