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rs879255314

From SNPedia

Orientationminus
Geno Mag Summary
(AGAAT;AGAAT) 0 common in clinvar
Make rs879255314(-;-)
Make rs879255314(-;AGAAT)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43093905
GeneBRCA1
is asnp
is mentioned by
dbSNPrs879255314
ebirs879255314
HLIrs879255314
Exacrs879255314
Varsomers879255314
Maprs879255314
PheGenIrs879255314
hapmaprs879255314
1000 genomesrs879255314
hgdprs879255314
ensemblrs879255314
gopubmedrs879255314
geneviewrs879255314
scholarrs879255314
googlers879255314
pharmgkbrs879255314
gwascentralrs879255314
openSNPrs879255314
23andMers879255314
23andMe allrs879255314
SNP Nexus

SNPshotrs879255314
SNPdbers879255314
MSV3drs879255314
GWAS Ctlgrs879255314
Max Magnitude0
ClinVar
Risk rs879255314(;)
Alt rs879255314(;)
Reference rs879255314(AGAAT;AGAAT)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene BRCA1
CLNDBN not specified
Reversed 1
HGVS NC_000017.10:g.41245922_41245926delATTCT
CLNSRC
CLNACC RCV000238673.1,