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rs1060499818

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs1060499818(-;-)
Make rs1060499818(-;TT)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23630336
GenePALB2
is asnp
is mentioned by
dbSNPrs1060499818
dbSNP (classic)rs1060499818
ClinGenrs1060499818
ebirs1060499818
HLIrs1060499818
Exacrs1060499818
Gnomadrs1060499818
Varsomers1060499818
LitVarrs1060499818
Maprs1060499818
PheGenIrs1060499818
Biobankrs1060499818
1000 genomesrs1060499818
hgdprs1060499818
ensemblrs1060499818
geneviewrs1060499818
scholarrs1060499818
googlers1060499818
pharmgkbrs1060499818
gwascentralrs1060499818
openSNPrs1060499818
23andMers1060499818
23andMe allrs1060499818
SNPshotrs1060499818
SNPdbers1060499818
MSV3drs1060499818
GWAS Ctlgrs1060499818
Max Magnitude0
ClinVar
Risk rs1060499818(-;-)
Alt rs1060499818(-;-)
Reference Rs1060499818(TT;TT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23641657_23641658delAA
CLNSRC
CLNACC RCV000454322.1,