Have questions? Visit https://www.reddit.com/r/SNPedia

rs1060499814

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499814(A;A)
Make rs1060499814(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23638069
GenePALB2
is asnp
is mentioned by
dbSNPrs1060499814
dbSNP (old)rs1060499814
ClinGenrs1060499814
ebirs1060499814
HLIrs1060499814
Exacrs1060499814
Gnomadrs1060499814
Varsomers1060499814
Maprs1060499814
PheGenIrs1060499814
Biobankrs1060499814
1000 genomesrs1060499814
hgdprs1060499814
ensemblrs1060499814
gopubmedrs1060499814
geneviewrs1060499814
scholarrs1060499814
googlers1060499814
pharmgkbrs1060499814
gwascentralrs1060499814
openSNPrs1060499814
23andMers1060499814
23andMe allrs1060499814
SNPshotrs1060499814
SNPdbers1060499814
MSV3drs1060499814
GWAS Ctlgrs1060499814
Max Magnitude0
ClinVar
Risk rs1060499814(A;A)
Alt rs1060499814(A;A)
Reference Rs1060499814(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Reversed 1
HGVS NC_000016.9:g.23649390C>T
CLNSRC
CLNACC RCV000454354.1, RCV000466548.1, RCV000484652.1,