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rs786202919

From SNPedia

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


Make rs786202919(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43093123
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786202919
ClinGenrs786202919
ebirs786202919
HLIrs786202919
Exacrs786202919
Varsomers786202919
Maprs786202919
PheGenIrs786202919
hapmaprs786202919
1000 genomesrs786202919
hgdprs786202919
ensemblrs786202919
gopubmedrs786202919
geneviewrs786202919
scholarrs786202919
googlers786202919
pharmgkbrs786202919
gwascentralrs786202919
openSNPrs786202919
23andMers786202919
23andMe allrs786202919
SNP Nexus

SNPshotrs786202919
SNPdbers786202919
MSV3drs786202919
GWAS Ctlgrs786202919
Max Magnitude6
ClinVar
Risk rs786202919(-;-)
Alt rs786202919(-;-)
Reference Rs786202919(AG;AG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41245140_41245141delCT
CLNSRC
CLNACC RCV000165987.1, RCV000241284.1,