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rs1057517539

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517539(A;A)
Make rs1057517539(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23629214
GenePALB2
is asnp
is mentioned by
dbSNPrs1057517539
dbSNP (classic)rs1057517539
ClinGenrs1057517539
ebirs1057517539
HLIrs1057517539
Exacrs1057517539
Gnomadrs1057517539
Varsomers1057517539
LitVarrs1057517539
Maprs1057517539
PheGenIrs1057517539
Biobankrs1057517539
1000 genomesrs1057517539
hgdprs1057517539
ensemblrs1057517539
geneviewrs1057517539
scholarrs1057517539
googlers1057517539
pharmgkbrs1057517539
gwascentralrs1057517539
openSNPrs1057517539
23andMers1057517539
23andMe allrs1057517539
SNPshotrs1057517539
SNPdbers1057517539
MSV3drs1057517539
GWAS Ctlgrs1057517539
Max Magnitude0
ClinVar
Risk rs1057517539(A;A)
Alt rs1057517539(A;A)
Reference Rs1057517539(C;C)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23640535G>T
CLNSRC
CLNACC RCV000410429.1, RCV000454290.1,