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rs1060502787

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502787(A;C)
Make rs1060502787(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23626399
GenePALB2
is asnp
is mentioned by
dbSNPrs1060502787
dbSNP (old)rs1060502787
ClinGenrs1060502787
ebirs1060502787
HLIrs1060502787
Exacrs1060502787
Gnomadrs1060502787
Varsomers1060502787
Maprs1060502787
PheGenIrs1060502787
Biobankrs1060502787
1000 genomesrs1060502787
hgdprs1060502787
ensemblrs1060502787
gopubmedrs1060502787
geneviewrs1060502787
scholarrs1060502787
googlers1060502787
pharmgkbrs1060502787
gwascentralrs1060502787
openSNPrs1060502787
23andMers1060502787
23andMe allrs1060502787
SNPshotrs1060502787
SNPdbers1060502787
MSV3drs1060502787
GWAS Ctlgrs1060502787
Max Magnitude0
ClinVar
Risk rs1060502787(C;C)
Alt rs1060502787(C;C)
Reference Rs1060502787(A;A)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23637720T>G
CLNSRC
CLNACC RCV000460478.1,