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rs1060499823

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499823(-;-)
Make rs1060499823(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23624011
GenePALB2
is asnp
is mentioned by
dbSNPrs1060499823
dbSNP (old)rs1060499823
ClinGenrs1060499823
ebirs1060499823
HLIrs1060499823
Exacrs1060499823
Gnomadrs1060499823
Varsomers1060499823
Maprs1060499823
PheGenIrs1060499823
Biobankrs1060499823
1000 genomesrs1060499823
hgdprs1060499823
ensemblrs1060499823
gopubmedrs1060499823
geneviewrs1060499823
scholarrs1060499823
googlers1060499823
pharmgkbrs1060499823
gwascentralrs1060499823
openSNPrs1060499823
23andMers1060499823
23andMe allrs1060499823
SNPshotrs1060499823
SNPdbers1060499823
MSV3drs1060499823
GWAS Ctlgrs1060499823
Max Magnitude0
ClinVar
Risk rs1060499823(-;-)
Alt rs1060499823(-;-)
Reference Rs1060499823(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23635332delG
CLNSRC
CLNACC RCV000454241.1,