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rs878853644

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853644(-;-)
Make rs878853644(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position21974677
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs878853644
ebirs878853644
HLIrs878853644
Exacrs878853644
Varsomers878853644
Maprs878853644
PheGenIrs878853644
hapmaprs878853644
1000 genomesrs878853644
hgdprs878853644
ensemblrs878853644
gopubmedrs878853644
geneviewrs878853644
scholarrs878853644
googlers878853644
pharmgkbrs878853644
gwascentralrs878853644
openSNPrs878853644
23andMers878853644
23andMe allrs878853644
SNP Nexus

SNPshotrs878853644
SNPdbers878853644
MSV3drs878853644
GWAS Ctlgrs878853644
Max Magnitude0
ClinVar
Risk rs878853644(;)
Alt rs878853644(;)
Reference rs878853644(G;G)
Significance Probable-Pathogenic
Disease Hereditary cutaneous melanoma
Variation info
Gene CDKN2A
CLNDBN Hereditary cutaneous melanoma
Reversed 1
HGVS NC_000009.11:g.21974676delC
CLNSRC
CLNACC RCV000234329.1,