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rs1060502356

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GTAAAG;GTAAAG) 0 common in clinvar
Make rs1060502356(-;-)
Make rs1060502356(-;GTAAAG)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position43057046
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1060502356
dbSNP (classic)rs1060502356
ClinGenrs1060502356
ebirs1060502356
HLIrs1060502356
Exacrs1060502356
Gnomadrs1060502356
Varsomers1060502356
LitVarrs1060502356
Maprs1060502356
PheGenIrs1060502356
Biobankrs1060502356
1000 genomesrs1060502356
hgdprs1060502356
ensemblrs1060502356
geneviewrs1060502356
scholarrs1060502356
googlers1060502356
pharmgkbrs1060502356
gwascentralrs1060502356
openSNPrs1060502356
23andMers1060502356
23andMe allrs1060502356
SNPshotrs1060502356
SNPdbers1060502356
MSV3drs1060502356
GWAS Ctlgrs1060502356
Max Magnitude0
ClinVar
Risk rs1060502356(-;-)
Alt rs1060502356(-;-)
Reference Rs1060502356(GTAAAG;GTAAAG)
Significance Probable-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.41209063_41209068delCTTTAC
CLNSRC
CLNACC RCV000463038.1,