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rs786202545

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786202545(A;G)
Make rs786202545(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43063375
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786202545
ebirs786202545
HLIrs786202545
Exacrs786202545
Varsomers786202545
Maprs786202545
PheGenIrs786202545
hapmaprs786202545
1000 genomesrs786202545
hgdprs786202545
ensemblrs786202545
gopubmedrs786202545
geneviewrs786202545
scholarrs786202545
googlers786202545
pharmgkbrs786202545
gwascentralrs786202545
openSNPrs786202545
23andMers786202545
23andMe allrs786202545
SNP Nexus

SNPshotrs786202545
SNPdbers786202545
MSV3drs786202545
GWAS Ctlgrs786202545
Max Magnitude0
ClinVar
Risk rs786202545(G;G)
Alt rs786202545(G;G)
Reference rs786202545(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41215392T>C
CLNSRC
CLNACC RCV000165403.1,