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rs786202646

From SNPedia

Merged intors753153576
Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202646(A;A)
Make rs786202646(A;C)
Make rs786202646(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23626235
GenePALB2
is asnp
is mentioned by
dbSNPrs786202646
ebirs786202646
HLIrs786202646
Exacrs786202646
Varsomers786202646
Maprs786202646
PheGenIrs786202646
hapmaprs786202646
1000 genomesrs786202646
hgdprs786202646
ensemblrs786202646
gopubmedrs786202646
geneviewrs786202646
scholarrs786202646
googlers786202646
pharmgkbrs786202646
gwascentralrs786202646
openSNPrs786202646
23andMers786202646
23andMe allrs786202646
SNP Nexus

SNPshotrs786202646
SNPdbers786202646
MSV3drs786202646
GWAS Ctlgrs786202646
StatusMerged into rs753153576
Max Magnitude0
ClinVar
Risk rs786202646(T;T)
Alt rs786202646(T;T)
Reference rs786202646(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.10:g.23626235C>A
CLNSRC
CLNACC RCV000165555.1,