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rs1057517600

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517600(-;-)
Make rs1057517600(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23607958
GenePALB2
is asnp
is mentioned by
dbSNPrs1057517600
dbSNP (classic)rs1057517600
ClinGenrs1057517600
ebirs1057517600
HLIrs1057517600
Exacrs1057517600
Gnomadrs1057517600
Varsomers1057517600
LitVarrs1057517600
Maprs1057517600
PheGenIrs1057517600
Biobankrs1057517600
1000 genomesrs1057517600
hgdprs1057517600
ensemblrs1057517600
geneviewrs1057517600
scholarrs1057517600
googlers1057517600
pharmgkbrs1057517600
gwascentralrs1057517600
openSNPrs1057517600
23andMers1057517600
SNPshotrs1057517600
SNPdbers1057517600
MSV3drs1057517600
GWAS Ctlgrs1057517600
Max Magnitude0
ClinVar
Risk rs1057517600(-;-)
Alt rs1057517600(-;-)
Reference Rs1057517600(C;C)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23619279delG
CLNSRC
CLNACC RCV000410678.1,