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rs397508941

From SNPedia

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


Make rs397508941(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093363
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508941
dbSNP (old)rs397508941
ClinGenrs397508941
ebirs397508941
HLIrs397508941
Exacrs397508941
Varsomers397508941
Maprs397508941
PheGenIrs397508941
Biobankrs397508941
1000 genomesrs397508941
hgdprs397508941
ensemblrs397508941
gopubmedrs397508941
geneviewrs397508941
scholarrs397508941
googlers397508941
pharmgkbrs397508941
gwascentralrs397508941
openSNPrs397508941
23andMers397508941
23andMe allrs397508941
SNP Nexus

SNPshotrs397508941
SNPdbers397508941
MSV3drs397508941
GWAS Ctlgrs397508941
Max Magnitude6
ClinVar
Risk rs397508941(-;-)
Alt rs397508941(-;-)
Reference Rs397508941(AAAGAATTTGTCAA;AAAGAATTTGTCAA)
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.41245380_41245393delTTGACAAATTCTTT
CLNSRC ClinVar
CLNACC RCV000047734.2, RCV000256818.2,