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rs1060499812

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499812(G;T)
Make rs1060499812(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23635507
GenePALB2
is asnp
is mentioned by
dbSNPrs1060499812
dbSNP (old)rs1060499812
ClinGenrs1060499812
ebirs1060499812
HLIrs1060499812
Exacrs1060499812
Gnomadrs1060499812
Varsomers1060499812
Maprs1060499812
PheGenIrs1060499812
Biobankrs1060499812
1000 genomesrs1060499812
hgdprs1060499812
ensemblrs1060499812
gopubmedrs1060499812
geneviewrs1060499812
scholarrs1060499812
googlers1060499812
pharmgkbrs1060499812
gwascentralrs1060499812
openSNPrs1060499812
23andMers1060499812
23andMe allrs1060499812
SNPshotrs1060499812
SNPdbers1060499812
MSV3drs1060499812
GWAS Ctlgrs1060499812
Max Magnitude0
ClinVar
Risk rs1060499812(T;T)
Alt rs1060499812(T;T)
Reference Rs1060499812(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23646828C>A
CLNSRC
CLNACC RCV000454356.1,