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rs587776480

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GTTTG;GTTTG) 0 common in clinvar
Make rs587776480(-;-)
Make rs587776480(-;GTTTG)
ReferenceGRCh38 38.1/142
Chromosome17
Position43093915
GeneBRCA1
is asnp
is mentioned by
dbSNPrs587776480
ebirs587776480
HLIrs587776480
Exacrs587776480
Varsomers587776480
Maprs587776480
PheGenIrs587776480
hapmaprs587776480
1000 genomesrs587776480
hgdprs587776480
ensemblrs587776480
gopubmedrs587776480
geneviewrs587776480
scholarrs587776480
googlers587776480
pharmgkbrs587776480
gwascentralrs587776480
openSNPrs587776480
23andMers587776480
23andMe allrs587776480
SNP Nexus

SNPshotrs587776480
SNPdbers587776480
MSV3drs587776480
GWAS Ctlgrs587776480
Max Magnitude0
ClinVar
Risk rs587776480(;)
Alt rs587776480(;)
Reference rs587776480(GTTTG;GTTTG)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 0
HGVS NC_000017.10:g.41245932_41245936delGTTTG
CLNSRC ClinVar
CLNACC RCV000144201.1,