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rs876658888

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;TGTTGAA) 6 BRCA2 variant considered pathogenic for breast cancer
(GAATGTT;GAATGTT) 0 common in clinvar
(TGTTGAA;TGTTGAA) 0 common/normal


Make rs876658888(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339689
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658888
dbSNP (old)rs876658888
ClinGenrs876658888
ebirs876658888
HLIrs876658888
Exacrs876658888
Varsomers876658888
Maprs876658888
PheGenIrs876658888
Biobankrs876658888
1000 genomesrs876658888
hgdprs876658888
ensemblrs876658888
gopubmedrs876658888
geneviewrs876658888
scholarrs876658888
googlers876658888
pharmgkbrs876658888
gwascentralrs876658888
openSNPrs876658888
23andMers876658888
23andMe allrs876658888
SNP Nexus

SNPshotrs876658888
SNPdbers876658888
MSV3drs876658888
GWAS Ctlgrs876658888
Max Magnitude6
ClinVar
Risk rs876658888(-;-)
Alt rs876658888(-;-)
Reference Rs876658888(GAATGTT;GAATGTT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913826_32913832delTGTTGAA
CLNSRC
CLNACC RCV000218789.1, RCV000257009.1,