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rs1057520736

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520736(C;G)
Make rs1057520736(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23635098
GenePALB2
is asnp
is mentioned by
dbSNPrs1057520736
dbSNP (old)rs1057520736
ClinGenrs1057520736
ebirs1057520736
HLIrs1057520736
Exacrs1057520736
Gnomadrs1057520736
Varsomers1057520736
Maprs1057520736
PheGenIrs1057520736
Biobankrs1057520736
1000 genomesrs1057520736
hgdprs1057520736
ensemblrs1057520736
gopubmedrs1057520736
geneviewrs1057520736
scholarrs1057520736
googlers1057520736
pharmgkbrs1057520736
gwascentralrs1057520736
openSNPrs1057520736
23andMers1057520736
23andMe allrs1057520736
SNPshotrs1057520736
SNPdbers1057520736
MSV3drs1057520736
GWAS Ctlgrs1057520736
Max Magnitude0
ClinVar
Risk rs1057520736(G;G)
Alt rs1057520736(G;G)
Reference Rs1057520736(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PALB2
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.23646419G>C
CLNSRC
CLNACC RCV000421638.1,