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rs730881441

From SNPedia

Orientationminus
Geno Mag Summary
(GGCAGATG;GGCAGATG) 0 common in clinvar
Make rs730881441(-;-)
Make rs730881441(-;GGCAGATG)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position43045789
GeneBRCA1
is asnp
is mentioned by
dbSNPrs730881441
ebirs730881441
HLIrs730881441
Exacrs730881441
Varsomers730881441
Maprs730881441
PheGenIrs730881441
hapmaprs730881441
1000 genomesrs730881441
hgdprs730881441
ensemblrs730881441
gopubmedrs730881441
geneviewrs730881441
scholarrs730881441
googlers730881441
pharmgkbrs730881441
gwascentralrs730881441
openSNPrs730881441
23andMers730881441
23andMe allrs730881441
SNP Nexus

SNPshotrs730881441
SNPdbers730881441
MSV3drs730881441
GWAS Ctlgrs730881441
Max Magnitude0
ClinVar
Risk rs730881441(;)
Alt rs730881441(;)
Reference rs730881441(GGCAGATG;GGCAGATG)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41197806_41197813delCATCTGCC
CLNSRC
CLNACC RCV000159845.1, RCV000163754.1,