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rs1060499817

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs1060499817(-;-)
Make rs1060499817(-;TT)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23634954
GenePALB2
is asnp
is mentioned by
dbSNPrs1060499817
dbSNP (old)rs1060499817
ClinGenrs1060499817
ebirs1060499817
HLIrs1060499817
Exacrs1060499817
Gnomadrs1060499817
Varsomers1060499817
LitVarrs1060499817
Maprs1060499817
PheGenIrs1060499817
Biobankrs1060499817
1000 genomesrs1060499817
hgdprs1060499817
ensemblrs1060499817
gopubmedrs1060499817
geneviewrs1060499817
scholarrs1060499817
googlers1060499817
pharmgkbrs1060499817
gwascentralrs1060499817
openSNPrs1060499817
23andMers1060499817
23andMe allrs1060499817
SNPshotrs1060499817
SNPdbers1060499817
MSV3drs1060499817
GWAS Ctlgrs1060499817
Max Magnitude0
ClinVar
Risk rs1060499817(-;-)
Alt rs1060499817(-;-)
Reference Rs1060499817(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.23646275_23646276delAA
CLNSRC
CLNACC RCV000454252.1,