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rs786204260

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204260(-;-)
Make rs786204260(-;G)
Make rs786204260(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43094290
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786204260
ebirs786204260
HLIrs786204260
Exacrs786204260
Varsomers786204260
Maprs786204260
PheGenIrs786204260
hapmaprs786204260
1000 genomesrs786204260
hgdprs786204260
ensemblrs786204260
gopubmedrs786204260
geneviewrs786204260
scholarrs786204260
googlers786204260
pharmgkbrs786204260
gwascentralrs786204260
openSNPrs786204260
23andMers786204260
23andMe allrs786204260
SNP Nexus

SNPshotrs786204260
SNPdbers786204260
MSV3drs786204260
GWAS Ctlgrs786204260
Max Magnitude0
ClinVar
Risk rs786204260(G;G)
Alt rs786204260(G;G)
Reference rs786204260(;)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 1
HGVS NC_000017.10:g.41246308dupC
CLNSRC
CLNACC RCV000168473.2,