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rs1060499821

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499821(C;C)
Make rs1060499821(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23626234
GenePALB2
is asnp
is mentioned by
dbSNPrs1060499821
dbSNP (classic)rs1060499821
ClinGenrs1060499821
ebirs1060499821
HLIrs1060499821
Exacrs1060499821
Gnomadrs1060499821
Varsomers1060499821
LitVarrs1060499821
Maprs1060499821
PheGenIrs1060499821
Biobankrs1060499821
1000 genomesrs1060499821
hgdprs1060499821
ensemblrs1060499821
geneviewrs1060499821
scholarrs1060499821
googlers1060499821
pharmgkbrs1060499821
gwascentralrs1060499821
openSNPrs1060499821
23andMers1060499821
23andMe allrs1060499821
SNPshotrs1060499821
SNPdbers1060499821
MSV3drs1060499821
GWAS Ctlgrs1060499821
Max Magnitude0
ClinVar
Risk rs1060499821(C;C)
Alt rs1060499821(C;C)
Reference Rs1060499821(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23637555A>G
CLNSRC
CLNACC RCV000454214.1,