Have questions? Visit https://www.reddit.com/r/SNPedia

rs1060502788

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502788(C;T)
Make rs1060502788(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23635498
GenePALB2
is asnp
is mentioned by
dbSNPrs1060502788
dbSNP (classic)rs1060502788
ClinGenrs1060502788
ebirs1060502788
HLIrs1060502788
Exacrs1060502788
Gnomadrs1060502788
Varsomers1060502788
LitVarrs1060502788
Maprs1060502788
PheGenIrs1060502788
Biobankrs1060502788
1000 genomesrs1060502788
hgdprs1060502788
ensemblrs1060502788
geneviewrs1060502788
scholarrs1060502788
googlers1060502788
pharmgkbrs1060502788
gwascentralrs1060502788
openSNPrs1060502788
23andMers1060502788
23andMe allrs1060502788
SNPshotrs1060502788
SNPdbers1060502788
MSV3drs1060502788
GWAS Ctlgrs1060502788
Max Magnitude0
ClinVar
Risk rs1060502788(T;T)
Alt rs1060502788(T;T)
Reference Rs1060502788(C;C)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23646819G>A
CLNSRC
CLNACC RCV000476491.1,