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rs869312774

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312774(-;-)
Make rs869312774(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23614019
GenePALB2
is asnp
is mentioned by
dbSNPrs869312774
ebirs869312774
HLIrs869312774
Exacrs869312774
Varsomers869312774
Maprs869312774
PheGenIrs869312774
hapmaprs869312774
1000 genomesrs869312774
hgdprs869312774
ensemblrs869312774
gopubmedrs869312774
geneviewrs869312774
scholarrs869312774
googlers869312774
pharmgkbrs869312774
gwascentralrs869312774
openSNPrs869312774
23andMers869312774
23andMe allrs869312774
SNP Nexus

SNPshotrs869312774
SNPdbers869312774
MSV3drs869312774
GWAS Ctlgrs869312774
Max Magnitude0
ClinVar
Risk rs869312774(;)
Alt rs869312774(;)
Reference rs869312774(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23625340delT
CLNSRC
CLNACC RCV000210123.1,