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rs1057520653

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520653(A;T)
Make rs1057520653(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23635108
GenePALB2
is asnp
is mentioned by
dbSNPrs1057520653
dbSNP (old)rs1057520653
ClinGenrs1057520653
ebirs1057520653
HLIrs1057520653
Exacrs1057520653
Gnomadrs1057520653
Varsomers1057520653
Maprs1057520653
PheGenIrs1057520653
Biobankrs1057520653
1000 genomesrs1057520653
hgdprs1057520653
ensemblrs1057520653
gopubmedrs1057520653
geneviewrs1057520653
scholarrs1057520653
googlers1057520653
pharmgkbrs1057520653
gwascentralrs1057520653
openSNPrs1057520653
23andMers1057520653
23andMe allrs1057520653
SNPshotrs1057520653
SNPdbers1057520653
MSV3drs1057520653
GWAS Ctlgrs1057520653
Max Magnitude0
ClinVar
Risk rs1057520653(T;T)
Alt rs1057520653(T;T)
Reference Rs1057520653(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PALB2
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.23646429T>A
CLNSRC
CLNACC RCV000424678.1,