Have questions? Visit https://www.reddit.com/r/SNPedia

rs876659571

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TGAA;TGAA) 0 common in clinvar
Make rs876659571(-;-)
Make rs876659571(-;TGAA)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23629863
GenePALB2
is asnp
is mentioned by
dbSNPrs876659571
dbSNP (classic)rs876659571
ClinGenrs876659571
ebirs876659571
HLIrs876659571
Exacrs876659571
Gnomadrs876659571
Varsomers876659571
LitVarrs876659571
Maprs876659571
PheGenIrs876659571
Biobankrs876659571
1000 genomesrs876659571
hgdprs876659571
ensemblrs876659571
geneviewrs876659571
scholarrs876659571
googlers876659571
pharmgkbrs876659571
gwascentralrs876659571
openSNPrs876659571
23andMers876659571
SNPshotrs876659571
SNPdbers876659571
MSV3drs876659571
GWAS Ctlgrs876659571
Max Magnitude0
ClinVar
Risk rs876659571(-;-)
Alt rs876659571(-;-)
Reference Rs876659571(TGAA;TGAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23641184_23641187delTTCA
CLNSRC
CLNACC RCV000213608.1, RCV000235354.1, RCV000467619.1,