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rs1060499829

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499829(-;-)
Make rs1060499829(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23641109
GeneDCTN5, PALB2
is asnp
is mentioned by
dbSNPrs1060499829
dbSNP (old)rs1060499829
ClinGenrs1060499829
ebirs1060499829
HLIrs1060499829
Exacrs1060499829
Gnomadrs1060499829
Varsomers1060499829
Maprs1060499829
PheGenIrs1060499829
Biobankrs1060499829
1000 genomesrs1060499829
hgdprs1060499829
ensemblrs1060499829
gopubmedrs1060499829
geneviewrs1060499829
scholarrs1060499829
googlers1060499829
pharmgkbrs1060499829
gwascentralrs1060499829
openSNPrs1060499829
23andMers1060499829
23andMe allrs1060499829
SNPshotrs1060499829
SNPdbers1060499829
MSV3drs1060499829
GWAS Ctlgrs1060499829
Max Magnitude0
ClinVar
Risk rs1060499829(-;-)
Alt rs1060499829(-;-)
Reference Rs1060499829(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2 DCTN5
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23652430delC
CLNSRC
CLNACC RCV000454282.1,