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rs786204267

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204267(-;-)
Make rs786204267(-;A)
Make rs786204267(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43076585
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786204267
ebirs786204267
HLIrs786204267
Exacrs786204267
Varsomers786204267
Maprs786204267
PheGenIrs786204267
hapmaprs786204267
1000 genomesrs786204267
hgdprs786204267
ensemblrs786204267
gopubmedrs786204267
geneviewrs786204267
scholarrs786204267
googlers786204267
pharmgkbrs786204267
gwascentralrs786204267
openSNPrs786204267
23andMers786204267
23andMe allrs786204267
SNP Nexus

SNPshotrs786204267
SNPdbers786204267
MSV3drs786204267
GWAS Ctlgrs786204267
Max Magnitude0
ClinVar
Risk rs786204267(A;A)
Alt rs786204267(A;A)
Reference rs786204267(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41228603dupT
CLNSRC
CLNACC RCV000168509.1,