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rs1060502362

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(GTCCAACT;GTCCAACT) 0 common in clinvar
Make rs1060502362(-;-)
Make rs1060502362(-;GTCCAACT)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position43099855
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1060502362
dbSNP (old)rs1060502362
ClinGenrs1060502362
ebirs1060502362
HLIrs1060502362
Exacrs1060502362
Gnomadrs1060502362
Varsomers1060502362
Maprs1060502362
PheGenIrs1060502362
Biobankrs1060502362
1000 genomesrs1060502362
hgdprs1060502362
ensemblrs1060502362
gopubmedrs1060502362
geneviewrs1060502362
scholarrs1060502362
googlers1060502362
pharmgkbrs1060502362
gwascentralrs1060502362
openSNPrs1060502362
23andMers1060502362
23andMe allrs1060502362
SNPshotrs1060502362
SNPdbers1060502362
MSV3drs1060502362
GWAS Ctlgrs1060502362
Max Magnitude0
ClinVar
Risk rs1060502362(-;-)
Alt rs1060502362(-;-)
Reference Rs1060502362(GTCCAACT;GTCCAACT)
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.41251872_41251879delAGTTGGAC
CLNSRC
CLNACC RCV000469427.1,