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rs587778587

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778587(A;A)
Make rs587778587(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23629645
GenePALB2
is asnp
is mentioned by
dbSNPrs587778587
ebirs587778587
HLIrs587778587
Exacrs587778587
Varsomers587778587
Maprs587778587
PheGenIrs587778587
hapmaprs587778587
1000 genomesrs587778587
hgdprs587778587
ensemblrs587778587
gopubmedrs587778587
geneviewrs587778587
scholarrs587778587
googlers587778587
pharmgkbrs587778587
gwascentralrs587778587
openSNPrs587778587
23andMers587778587
23andMe allrs587778587
SNP Nexus

SNPshotrs587778587
SNPdbers587778587
MSV3drs587778587
GWAS Ctlgrs587778587
Max Magnitude0
ClinVar
Risk rs587778587(A;A)
Alt rs587778587(A;A)
Reference rs587778587(G;G)
Significance Pathogenic
Disease Familial cancer of breast not provided Hereditary cancer-predisposing syndrome not specified
Variation info
Gene PALB2
CLNDBN Familial cancer of breast not provided Hereditary cancer-predisposing syndrome not specified
Reversed 1
HGVS NC_000016.9:g.23640966C>A; NC_000016.9:g.23640966C>T
CLNSRC
CLNACC RCV000227927.1, RCV000235331.1, RCV000116087.5, RCV000121758.1, RCV000232962.1,