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rs1060499824

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499824(-;-)
Make rs1060499824(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23623115
GenePALB2
is asnp
is mentioned by
dbSNPrs1060499824
dbSNP (old)rs1060499824
ClinGenrs1060499824
ebirs1060499824
HLIrs1060499824
Exacrs1060499824
Gnomadrs1060499824
Varsomers1060499824
LitVarrs1060499824
Maprs1060499824
PheGenIrs1060499824
Biobankrs1060499824
1000 genomesrs1060499824
hgdprs1060499824
ensemblrs1060499824
gopubmedrs1060499824
geneviewrs1060499824
scholarrs1060499824
googlers1060499824
pharmgkbrs1060499824
gwascentralrs1060499824
openSNPrs1060499824
23andMers1060499824
23andMe allrs1060499824
SNPshotrs1060499824
SNPdbers1060499824
MSV3drs1060499824
GWAS Ctlgrs1060499824
Max Magnitude0
ClinVar
Risk rs1060499824(-;-)
Alt rs1060499824(-;-)
Reference Rs1060499824(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.23634436delG
CLNSRC
CLNACC RCV000454187.1,