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

rs876659253

From SNPedia

Orientationminus
Geno Mag Summary
(ATGT;ATGT) 0 common in clinvar
Make rs876659253(ATGT;CA)
Make rs876659253(CA;CA)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43094296
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659253
ebirs876659253
HLIrs876659253
Exacrs876659253
Varsomers876659253
Maprs876659253
PheGenIrs876659253
hapmaprs876659253
1000 genomesrs876659253
hgdprs876659253
ensemblrs876659253
gopubmedrs876659253
geneviewrs876659253
scholarrs876659253
googlers876659253
pharmgkbrs876659253
gwascentralrs876659253
openSNPrs876659253
23andMers876659253
23andMe allrs876659253
SNP Nexus

SNPshotrs876659253
SNPdbers876659253
MSV3drs876659253
GWAS Ctlgrs876659253
Max Magnitude0
ClinVar
Risk rs876659253(CA;CA)
Alt rs876659253(CA;CA)
Reference rs876659253(ATGT;ATGT)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.41246313_41246316delACATinsTG
CLNSRC
CLNACC RCV000218956.1,