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rs1060499827

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499827(A;C)
Make rs1060499827(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23608014
GenePALB2
is asnp
is mentioned by
dbSNPrs1060499827
dbSNP (old)rs1060499827
ClinGenrs1060499827
ebirs1060499827
HLIrs1060499827
Exacrs1060499827
Gnomadrs1060499827
Varsomers1060499827
Maprs1060499827
PheGenIrs1060499827
Biobankrs1060499827
1000 genomesrs1060499827
hgdprs1060499827
ensemblrs1060499827
gopubmedrs1060499827
geneviewrs1060499827
scholarrs1060499827
googlers1060499827
pharmgkbrs1060499827
gwascentralrs1060499827
openSNPrs1060499827
23andMers1060499827
23andMe allrs1060499827
SNPshotrs1060499827
SNPdbers1060499827
MSV3drs1060499827
GWAS Ctlgrs1060499827
Max Magnitude0
ClinVar
Risk rs1060499827(C;C)
Alt rs1060499827(C;C)
Reference Rs1060499827(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23619335T>G
CLNSRC
CLNACC RCV000454196.1,