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rs730881458

From SNPedia

Orientationminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs730881458(-;-)
Make rs730881458(-;TT)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position43094190
GeneBRCA1
is asnp
is mentioned by
dbSNPrs730881458
ebirs730881458
HLIrs730881458
Exacrs730881458
Varsomers730881458
Maprs730881458
PheGenIrs730881458
hapmaprs730881458
1000 genomesrs730881458
hgdprs730881458
ensemblrs730881458
gopubmedrs730881458
geneviewrs730881458
scholarrs730881458
googlers730881458
pharmgkbrs730881458
gwascentralrs730881458
openSNPrs730881458
23andMers730881458
23andMe allrs730881458
SNP Nexus

SNPshotrs730881458
SNPdbers730881458
MSV3drs730881458
GWAS Ctlgrs730881458
Max Magnitude0
ClinVar
Risk rs730881458(;)
Alt rs730881458(;)
Reference rs730881458(TT;TT)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246207_41246208delAA
CLNSRC
CLNACC RCV000159900.1,