Have questions? Visit https://www.reddit.com/r/SNPedia

rs587782792

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587782792(A;C)
Make rs587782792(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position21971108
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs587782792
ebirs587782792
HLIrs587782792
Exacrs587782792
Varsomers587782792
Maprs587782792
PheGenIrs587782792
hapmaprs587782792
1000 genomesrs587782792
hgdprs587782792
ensemblrs587782792
gopubmedrs587782792
geneviewrs587782792
scholarrs587782792
googlers587782792
pharmgkbrs587782792
gwascentralrs587782792
openSNPrs587782792
23andMers587782792
23andMe allrs587782792
SNP Nexus

SNPshotrs587782792
SNPdbers587782792
MSV3drs587782792
GWAS Ctlgrs587782792
Max Magnitude0
ClinVar
Risk rs587782792(C;C)
Alt rs587782792(C;C)
Reference rs587782792(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene CDKN2A
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000009.11:g.21971107T>G
CLNSRC
CLNACC RCV000132342.2, RCV000236474.1,