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rs1060499828

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499828(-;-)
Make rs1060499828(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23607903
GenePALB2
is asnp
is mentioned by
dbSNPrs1060499828
dbSNP (old)rs1060499828
ClinGenrs1060499828
ebirs1060499828
HLIrs1060499828
Exacrs1060499828
Gnomadrs1060499828
Varsomers1060499828
Maprs1060499828
PheGenIrs1060499828
Biobankrs1060499828
1000 genomesrs1060499828
hgdprs1060499828
ensemblrs1060499828
gopubmedrs1060499828
geneviewrs1060499828
scholarrs1060499828
googlers1060499828
pharmgkbrs1060499828
gwascentralrs1060499828
openSNPrs1060499828
23andMers1060499828
23andMe allrs1060499828
SNPshotrs1060499828
SNPdbers1060499828
MSV3drs1060499828
GWAS Ctlgrs1060499828
Max Magnitude0
ClinVar
Risk rs1060499828(-;-)
Alt rs1060499828(-;-)
Reference Rs1060499828(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000016.9:g.23619224delC
CLNSRC
CLNACC RCV000454312.1, RCV000484224.1,