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rs1060502333

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502333(-;-)
Make rs1060502333(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position43093322
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1060502333
dbSNP (old)rs1060502333
ClinGenrs1060502333
ebirs1060502333
HLIrs1060502333
Exacrs1060502333
Gnomadrs1060502333
Varsomers1060502333
Maprs1060502333
PheGenIrs1060502333
Biobankrs1060502333
1000 genomesrs1060502333
hgdprs1060502333
ensemblrs1060502333
gopubmedrs1060502333
geneviewrs1060502333
scholarrs1060502333
googlers1060502333
pharmgkbrs1060502333
gwascentralrs1060502333
openSNPrs1060502333
23andMers1060502333
23andMe allrs1060502333
SNPshotrs1060502333
SNPdbers1060502333
MSV3drs1060502333
GWAS Ctlgrs1060502333
Max Magnitude0
ClinVar
Risk rs1060502333(-;-)
Alt rs1060502333(-;-)
Reference Rs1060502333(A;A)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 1
HGVS NC_000017.10:g.41245339delT
CLNSRC
CLNACC RCV000461584.1,