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rs397509088

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509088(-;-)
Make rs397509088(-;A)
Make rs397509088(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091906
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509088
ebirs397509088
HLIrs397509088
Exacrs397509088
Varsomers397509088
Maprs397509088
PheGenIrs397509088
hapmaprs397509088
1000 genomesrs397509088
hgdprs397509088
ensemblrs397509088
gopubmedrs397509088
geneviewrs397509088
scholarrs397509088
googlers397509088
pharmgkbrs397509088
gwascentralrs397509088
openSNPrs397509088
23andMers397509088
23andMe allrs397509088
SNP Nexus

SNPshotrs397509088
SNPdbers397509088
MSV3drs397509088
GWAS Ctlgrs397509088
Max Magnitude0
ClinVar
Risk rs397509088(A;A)
Alt rs397509088(A;A)
Reference rs397509088(;)
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.41243924dupT
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048259.2, RCV000112139.1,