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rs1057517602

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517602(-;-)
Make rs1057517602(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23630316
GenePALB2
is asnp
is mentioned by
dbSNPrs1057517602
dbSNP (old)rs1057517602
ClinGenrs1057517602
ebirs1057517602
HLIrs1057517602
Exacrs1057517602
Gnomadrs1057517602
Varsomers1057517602
Maprs1057517602
PheGenIrs1057517602
Biobankrs1057517602
1000 genomesrs1057517602
hgdprs1057517602
ensemblrs1057517602
gopubmedrs1057517602
geneviewrs1057517602
scholarrs1057517602
googlers1057517602
pharmgkbrs1057517602
gwascentralrs1057517602
openSNPrs1057517602
23andMers1057517602
23andMe allrs1057517602
SNPshotrs1057517602
SNPdbers1057517602
MSV3drs1057517602
GWAS Ctlgrs1057517602
Max Magnitude0
ClinVar
Risk rs1057517602(-;-)
Alt rs1057517602(-;-)
Reference Rs1057517602(A;A)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23641637delT
CLNSRC
CLNACC RCV000411169.1,