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rs1060499830

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499830(-;-)
Make rs1060499830(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23635787
GenePALB2
is asnp
is mentioned by
dbSNPrs1060499830
dbSNP (old)rs1060499830
ClinGenrs1060499830
ebirs1060499830
HLIrs1060499830
Exacrs1060499830
Gnomadrs1060499830
Varsomers1060499830
Maprs1060499830
PheGenIrs1060499830
Biobankrs1060499830
1000 genomesrs1060499830
hgdprs1060499830
ensemblrs1060499830
gopubmedrs1060499830
geneviewrs1060499830
scholarrs1060499830
googlers1060499830
pharmgkbrs1060499830
gwascentralrs1060499830
openSNPrs1060499830
23andMers1060499830
23andMe allrs1060499830
SNPshotrs1060499830
SNPdbers1060499830
MSV3drs1060499830
GWAS Ctlgrs1060499830
Max Magnitude0
ClinVar
Risk rs1060499830(-;-)
Alt rs1060499830(-;-)
Reference Rs1060499830(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23647108delT
CLNSRC
CLNACC RCV000454341.1, RCV000458746.1,