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rs1060499819

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499819(-;-)
Make rs1060499819(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23630062
GenePALB2
is asnp
is mentioned by
dbSNPrs1060499819
dbSNP (old)rs1060499819
ClinGenrs1060499819
ebirs1060499819
HLIrs1060499819
Exacrs1060499819
Gnomadrs1060499819
Varsomers1060499819
Maprs1060499819
PheGenIrs1060499819
Biobankrs1060499819
1000 genomesrs1060499819
hgdprs1060499819
ensemblrs1060499819
gopubmedrs1060499819
geneviewrs1060499819
scholarrs1060499819
googlers1060499819
pharmgkbrs1060499819
gwascentralrs1060499819
openSNPrs1060499819
23andMers1060499819
23andMe allrs1060499819
SNPshotrs1060499819
SNPdbers1060499819
MSV3drs1060499819
GWAS Ctlgrs1060499819
Max Magnitude0
ClinVar
Risk rs1060499819(-;-)
Alt rs1060499819(-;-)
Reference Rs1060499819(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23641383delG
CLNSRC
CLNACC RCV000454277.1,