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rs778345761

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs778345761(C;T)
Make rs778345761(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23614091
GenePALB2
is asnp
is mentioned by
dbSNPrs778345761
dbSNP (old)rs778345761
ClinGenrs778345761
ebirs778345761
HLIrs778345761
Exacrs778345761
Varsomers778345761
Maprs778345761
PheGenIrs778345761
Biobankrs778345761
1000 genomesrs778345761
hgdprs778345761
ensemblrs778345761
gopubmedrs778345761
geneviewrs778345761
scholarrs778345761
googlers778345761
pharmgkbrs778345761
gwascentralrs778345761
openSNPrs778345761
23andMers778345761
23andMe allrs778345761
SNP Nexus

SNPshotrs778345761
SNPdbers778345761
MSV3drs778345761
GWAS Ctlgrs778345761
Max Magnitude0
ClinVar
Risk rs778345761(T;T)
Alt rs778345761(T;T)
Reference Rs778345761(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.23625412C>T
CLNSRC
CLNACC RCV000222262.2,