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rs1057520645

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520645(C;C)
Make rs1057520645(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23630470
GenePALB2
is asnp
is mentioned by
dbSNPrs1057520645
dbSNP (old)rs1057520645
ClinGenrs1057520645
ebirs1057520645
HLIrs1057520645
Exacrs1057520645
Gnomadrs1057520645
Varsomers1057520645
LitVarrs1057520645
Maprs1057520645
PheGenIrs1057520645
Biobankrs1057520645
1000 genomesrs1057520645
hgdprs1057520645
ensemblrs1057520645
gopubmedrs1057520645
geneviewrs1057520645
scholarrs1057520645
googlers1057520645
pharmgkbrs1057520645
gwascentralrs1057520645
openSNPrs1057520645
23andMers1057520645
23andMe allrs1057520645
SNPshotrs1057520645
SNPdbers1057520645
MSV3drs1057520645
GWAS Ctlgrs1057520645
Max Magnitude0
ClinVar
Risk rs1057520645(C;C)
Alt rs1057520645(C;C)
Reference Rs1057520645(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PALB2
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.23641791C>G
CLNSRC
CLNACC RCV000431972.1,