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rs876659139

From SNPedia

Orientationminus
Geno Mag Summary
(TAAAG;TAAAG) 0 common in clinvar
Make rs876659139(-;-)
Make rs876659139(-;TAAAG)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43094022
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659139
ebirs876659139
HLIrs876659139
Exacrs876659139
Varsomers876659139
Maprs876659139
PheGenIrs876659139
hapmaprs876659139
1000 genomesrs876659139
hgdprs876659139
ensemblrs876659139
gopubmedrs876659139
geneviewrs876659139
scholarrs876659139
googlers876659139
pharmgkbrs876659139
gwascentralrs876659139
openSNPrs876659139
23andMers876659139
23andMe allrs876659139
SNP Nexus

SNPshotrs876659139
SNPdbers876659139
MSV3drs876659139
GWAS Ctlgrs876659139
Max Magnitude0
ClinVar
Risk rs876659139(;)
Alt rs876659139(;)
Reference rs876659139(TAAAG;TAAAG)
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.41246039_41246043delCTTTA
CLNSRC
CLNACC RCV000218408.1,