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rs752592662

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs752592662(A;C)
Make rs752592662(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23630046
GenePALB2
is asnp
is mentioned by
dbSNPrs752592662
ebirs752592662
HLIrs752592662
Exacrs752592662
Varsomers752592662
Maprs752592662
PheGenIrs752592662
hapmaprs752592662
1000 genomesrs752592662
hgdprs752592662
ensemblrs752592662
gopubmedrs752592662
geneviewrs752592662
scholarrs752592662
googlers752592662
pharmgkbrs752592662
gwascentralrs752592662
openSNPrs752592662
23andMers752592662
23andMe allrs752592662
SNP Nexus

SNPshotrs752592662
SNPdbers752592662
MSV3drs752592662
GWAS Ctlgrs752592662
Max Magnitude0
ClinVar
Risk rs752592662(C;C)
Alt rs752592662(C;C)
Reference Rs752592662(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.23641367A>C
CLNSRC
CLNACC RCV000223583.1,