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rs786203884

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203884(G;G)
Make rs786203884(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43091905
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786203884
ebirs786203884
HLIrs786203884
Exacrs786203884
Varsomers786203884
Maprs786203884
PheGenIrs786203884
hapmaprs786203884
1000 genomesrs786203884
hgdprs786203884
ensemblrs786203884
gopubmedrs786203884
geneviewrs786203884
scholarrs786203884
googlers786203884
pharmgkbrs786203884
gwascentralrs786203884
openSNPrs786203884
23andMers786203884
23andMe allrs786203884
SNP Nexus

SNPshotrs786203884
SNPdbers786203884
MSV3drs786203884
GWAS Ctlgrs786203884
Max Magnitude0
ClinVar
Risk rs786203884(G;G)
Alt rs786203884(G;G)
Reference rs786203884(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41243922A>C
CLNSRC
CLNACC RCV000167384.1,