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rs879255318

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs879255318(-;-)
Make rs879255318(-;TGGAATC)
Make rs879255318(TGGAATC;TGGAATC)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43071209
GeneBRCA1
is asnp
is mentioned by
dbSNPrs879255318
ebirs879255318
HLIrs879255318
Exacrs879255318
Varsomers879255318
Maprs879255318
PheGenIrs879255318
hapmaprs879255318
1000 genomesrs879255318
hgdprs879255318
ensemblrs879255318
gopubmedrs879255318
geneviewrs879255318
scholarrs879255318
googlers879255318
pharmgkbrs879255318
gwascentralrs879255318
openSNPrs879255318
23andMers879255318
23andMe allrs879255318
SNP Nexus

SNPshotrs879255318
SNPdbers879255318
MSV3drs879255318
GWAS Ctlgrs879255318
Max Magnitude0
ClinVar
Risk rs879255318(TGGAATC;TGGAATC)
Alt rs879255318(TGGAATC;TGGAATC)
Reference rs879255318(;)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene BRCA1
CLNDBN not specified
Reversed 1
HGVS NC_000017.10:g.41223227_41223233dupGATTCCA
CLNSRC
CLNACC RCV000238727.1,