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

rs878853650

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853650(C;C)
Make rs878853650(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position21974733
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs878853650
ebirs878853650
HLIrs878853650
Exacrs878853650
Varsomers878853650
Maprs878853650
PheGenIrs878853650
hapmaprs878853650
1000 genomesrs878853650
hgdprs878853650
ensemblrs878853650
gopubmedrs878853650
geneviewrs878853650
scholarrs878853650
googlers878853650
pharmgkbrs878853650
gwascentralrs878853650
openSNPrs878853650
23andMers878853650
23andMe allrs878853650
SNP Nexus

SNPshotrs878853650
SNPdbers878853650
MSV3drs878853650
GWAS Ctlgrs878853650
Max Magnitude0
ClinVar
Risk rs878853650(C;C)
Alt rs878853650(C;C)
Reference rs878853650(T;T)
Significance Probable-Pathogenic
Disease Hereditary cutaneous melanoma
Variation info
Gene CDKN2A
CLNDBN Hereditary cutaneous melanoma
Reversed 1
HGVS NC_000009.11:g.21974732A>G
CLNSRC
CLNACC RCV000234305.1,