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rs786202906

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786202906(-;-)
Make rs786202906(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43092465
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786202906
ebirs786202906
HLIrs786202906
Exacrs786202906
Varsomers786202906
Maprs786202906
PheGenIrs786202906
hapmaprs786202906
1000 genomesrs786202906
hgdprs786202906
ensemblrs786202906
gopubmedrs786202906
geneviewrs786202906
scholarrs786202906
googlers786202906
pharmgkbrs786202906
gwascentralrs786202906
openSNPrs786202906
23andMers786202906
23andMe allrs786202906
SNP Nexus

SNPshotrs786202906
SNPdbers786202906
MSV3drs786202906
GWAS Ctlgrs786202906
Max Magnitude0
ClinVar
Risk rs786202906(;)
Alt rs786202906(;)
Reference rs786202906(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41244482delT
CLNSRC
CLNACC RCV000165967.1,