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rs879255313

From SNPedia

Orientationminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs879255313(-;-)
Make rs879255313(-;AA)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43094388
GeneBRCA1
is asnp
is mentioned by
dbSNPrs879255313
ebirs879255313
HLIrs879255313
Exacrs879255313
Varsomers879255313
Maprs879255313
PheGenIrs879255313
hapmaprs879255313
1000 genomesrs879255313
hgdprs879255313
ensemblrs879255313
gopubmedrs879255313
geneviewrs879255313
scholarrs879255313
googlers879255313
pharmgkbrs879255313
gwascentralrs879255313
openSNPrs879255313
23andMers879255313
23andMe allrs879255313
SNP Nexus

SNPshotrs879255313
SNPdbers879255313
MSV3drs879255313
GWAS Ctlgrs879255313
Max Magnitude0
ClinVar
Risk rs879255313(;)
Alt rs879255313(;)
Reference rs879255313(AA;AA)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene BRCA1
CLNDBN not specified
Reversed 1
HGVS NC_000017.10:g.41246405_41246406delTT
CLNSRC
CLNACC RCV000239120.1,