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rs876660492

From SNPedia

Orientationminus
Geno Mag Summary
(GACTTCTGGA;GACTTCTGGA) 0 common in clinvar
Make rs876660492(-;-)
Make rs876660492(-;GACTTCTGGA)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23603615
GenePALB2
is asnp
is mentioned by
dbSNPrs876660492
ebirs876660492
HLIrs876660492
Exacrs876660492
Varsomers876660492
Maprs876660492
PheGenIrs876660492
hapmaprs876660492
1000 genomesrs876660492
hgdprs876660492
ensemblrs876660492
gopubmedrs876660492
geneviewrs876660492
scholarrs876660492
googlers876660492
pharmgkbrs876660492
gwascentralrs876660492
openSNPrs876660492
23andMers876660492
23andMe allrs876660492
SNP Nexus

SNPshotrs876660492
SNPdbers876660492
MSV3drs876660492
GWAS Ctlgrs876660492
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs876660492(GACTTCTGGA;GACTTCTGGA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23614936_23614945delTCCAGAAGTC
CLNSRC
CLNACC RCV000217312.1,