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rs786204261

From SNPedia

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


Make rs786204261(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43094645
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786204261
ClinGenrs786204261
ebirs786204261
HLIrs786204261
Exacrs786204261
Varsomers786204261
Maprs786204261
PheGenIrs786204261
hapmaprs786204261
1000 genomesrs786204261
hgdprs786204261
ensemblrs786204261
gopubmedrs786204261
geneviewrs786204261
scholarrs786204261
googlers786204261
pharmgkbrs786204261
gwascentralrs786204261
openSNPrs786204261
23andMers786204261
23andMe allrs786204261
SNP Nexus

SNPshotrs786204261
SNPdbers786204261
MSV3drs786204261
GWAS Ctlgrs786204261
Max Magnitude6
ClinVar
Risk rs786204261(-;-)
Alt rs786204261(-;-)
Reference Rs786204261(CA;CA)
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.41246662_41246663delTG
CLNSRC Children's Hospital of Eastern Ontario
CLNACC RCV000168487.3, RCV000257899.1,