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rs1060499813

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(TCAA;TCAA) 0 common in clinvar
Make rs1060499813(-;-)
Make rs1060499813(-;TCAA)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23635496
GenePALB2
is asnp
is mentioned by
dbSNPrs1060499813
dbSNP (old)rs1060499813
ClinGenrs1060499813
ebirs1060499813
HLIrs1060499813
Exacrs1060499813
Gnomadrs1060499813
Varsomers1060499813
Maprs1060499813
PheGenIrs1060499813
Biobankrs1060499813
1000 genomesrs1060499813
hgdprs1060499813
ensemblrs1060499813
gopubmedrs1060499813
geneviewrs1060499813
scholarrs1060499813
googlers1060499813
pharmgkbrs1060499813
gwascentralrs1060499813
openSNPrs1060499813
23andMers1060499813
23andMe allrs1060499813
SNPshotrs1060499813
SNPdbers1060499813
MSV3drs1060499813
GWAS Ctlgrs1060499813
Max Magnitude0
ClinVar
Risk rs1060499813(-;-)
Alt rs1060499813(-;-)
Reference Rs1060499813(TCAA;TCAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23646817_23646820delTTGA
CLNSRC
CLNACC RCV000454229.1,