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rs876658888

From SNPedia

Orientationplus
Geno Mag Summary
(GAATGTT;GAATGTT) 0 common in clinvar
Make rs876658888(-;-)
Make rs876658888(-;TGTTGAA)
Make rs876658888(TGTTGAA;TGTTGAA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339689
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658888
ebirs876658888
HLIrs876658888
Exacrs876658888
Varsomers876658888
Maprs876658888
PheGenIrs876658888
hapmaprs876658888
1000 genomesrs876658888
hgdprs876658888
ensemblrs876658888
gopubmedrs876658888
geneviewrs876658888
scholarrs876658888
googlers876658888
pharmgkbrs876658888
gwascentralrs876658888
openSNPrs876658888
23andMers876658888
23andMe allrs876658888
SNP Nexus

SNPshotrs876658888
SNPdbers876658888
MSV3drs876658888
GWAS Ctlgrs876658888
Max Magnitude0
ClinVar
Risk rs876658888(;)
Alt rs876658888(;)
Reference rs876658888(GAATGTT;GAATGTT)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32913826_32913832delTGTTGAA
CLNSRC
CLNACC RCV000218789.1,