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rs1060502327

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502327(-;-)
Make rs1060502327(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position43099877
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1060502327
dbSNP (old)rs1060502327
ClinGenrs1060502327
ebirs1060502327
HLIrs1060502327
Exacrs1060502327
Gnomadrs1060502327
Varsomers1060502327
LitVarrs1060502327
Maprs1060502327
PheGenIrs1060502327
Biobankrs1060502327
1000 genomesrs1060502327
hgdprs1060502327
ensemblrs1060502327
gopubmedrs1060502327
geneviewrs1060502327
scholarrs1060502327
googlers1060502327
pharmgkbrs1060502327
gwascentralrs1060502327
openSNPrs1060502327
23andMers1060502327
23andMe allrs1060502327
SNPshotrs1060502327
SNPdbers1060502327
MSV3drs1060502327
GWAS Ctlgrs1060502327
Max Magnitude0
ClinVar
Risk rs1060502327(-;-)
Alt rs1060502327(-;-)
Reference Rs1060502327(G;G)
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.41251894delC
CLNSRC
CLNACC RCV000467625.1,