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rs786203526

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203526(-;-)
Make rs786203526(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43106455
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786203526
ebirs786203526
HLIrs786203526
Exacrs786203526
Varsomers786203526
Maprs786203526
PheGenIrs786203526
hapmaprs786203526
1000 genomesrs786203526
hgdprs786203526
ensemblrs786203526
gopubmedrs786203526
geneviewrs786203526
scholarrs786203526
googlers786203526
pharmgkbrs786203526
gwascentralrs786203526
openSNPrs786203526
23andMers786203526
23andMe allrs786203526
SNP Nexus

SNPshotrs786203526
SNPdbers786203526
MSV3drs786203526
GWAS Ctlgrs786203526
Max Magnitude0
ClinVar
Risk rs786203526(;)
Alt rs786203526(;)
Reference rs786203526(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41258472delC
CLNSRC
CLNACC RCV000166870.1,