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

rs587782206

From SNPedia

Orientationminus
Geno Mag Summary
(TGGC;TGGC) 0 common in clinvar
Make rs587782206(-;-)
Make rs587782206(-;TGGC)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position21974778
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs587782206
ClinGenrs587782206
ebirs587782206
HLIrs587782206
Exacrs587782206
Varsomers587782206
Maprs587782206
PheGenIrs587782206
hapmaprs587782206
1000 genomesrs587782206
hgdprs587782206
ensemblrs587782206
gopubmedrs587782206
geneviewrs587782206
scholarrs587782206
googlers587782206
pharmgkbrs587782206
gwascentralrs587782206
openSNPrs587782206
23andMers587782206
23andMe allrs587782206
SNP Nexus

SNPshotrs587782206
SNPdbers587782206
MSV3drs587782206
GWAS Ctlgrs587782206
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs587782206(TGGC;TGGC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDKN2A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000009.11:g.21974777_21974780delGCCA
CLNSRC
CLNACC RCV000130872.3,