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rs786204267

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;A) 6 BRCA1 variant considered pathogenic for breast cancer
Make rs786204267(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43076585
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786204267
dbSNP (old)rs786204267
ClinGenrs786204267
ebirs786204267
HLIrs786204267
Exacrs786204267
Gnomadrs786204267
Varsomers786204267
Maprs786204267
PheGenIrs786204267
Biobankrs786204267
1000 genomesrs786204267
hgdprs786204267
ensemblrs786204267
gopubmedrs786204267
geneviewrs786204267
scholarrs786204267
googlers786204267
pharmgkbrs786204267
gwascentralrs786204267
openSNPrs786204267
23andMers786204267
23andMe allrs786204267
SNP Nexus

SNPshotrs786204267
SNPdbers786204267
MSV3drs786204267
GWAS Ctlgrs786204267
Max Magnitude6
ClinVar
Risk rs786204267(A;A)
Alt rs786204267(A;A)
Reference Rs786204267(-;-)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Hereditary breast and ovarian cancer syndrome
Reversed 1
HGVS NC_000017.10:g.41228603dupT
CLNSRC Children's Hospital of Eastern Ontario
CLNACC RCV000168509.3, RCV000257898.1,