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

rs1060499831

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499831(A;T)
Make rs1060499831(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23635615
GenePALB2
is asnp
is mentioned by
dbSNPrs1060499831
dbSNP (old)rs1060499831
ClinGenrs1060499831
ebirs1060499831
HLIrs1060499831
Exacrs1060499831
Gnomadrs1060499831
Varsomers1060499831
Maprs1060499831
PheGenIrs1060499831
Biobankrs1060499831
1000 genomesrs1060499831
hgdprs1060499831
ensemblrs1060499831
gopubmedrs1060499831
geneviewrs1060499831
scholarrs1060499831
googlers1060499831
pharmgkbrs1060499831
gwascentralrs1060499831
openSNPrs1060499831
23andMers1060499831
23andMe allrs1060499831
SNPshotrs1060499831
SNPdbers1060499831
MSV3drs1060499831
GWAS Ctlgrs1060499831
Max Magnitude0
ClinVar
Risk rs1060499831(T;T)
Alt rs1060499831(T;T)
Reference Rs1060499831(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23646936T>A
CLNSRC
CLNACC RCV000454180.1,