Have questions? Visit https://www.reddit.com/r/SNPedia

rs786202963

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202963(-;-)
Make rs786202963(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43091873
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786202963
ebirs786202963
HLIrs786202963
Exacrs786202963
Varsomers786202963
Maprs786202963
PheGenIrs786202963
hapmaprs786202963
1000 genomesrs786202963
hgdprs786202963
ensemblrs786202963
gopubmedrs786202963
geneviewrs786202963
scholarrs786202963
googlers786202963
pharmgkbrs786202963
gwascentralrs786202963
openSNPrs786202963
23andMers786202963
23andMe allrs786202963
SNP Nexus

SNPshotrs786202963
SNPdbers786202963
MSV3drs786202963
GWAS Ctlgrs786202963
Max Magnitude0
ClinVar
Risk rs786202963(;)
Alt rs786202963(;)
Reference rs786202963(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41243890delC
CLNSRC
CLNACC RCV000166048.1,