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rs559848002

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs559848002(C;C)
Make rs559848002(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position21971147
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs559848002
dbSNP (classic)rs559848002
ClinGenrs559848002
ebirs559848002
HLIrs559848002
Exacrs559848002
Gnomadrs559848002
Varsomers559848002
LitVarrs559848002
Maprs559848002
PheGenIrs559848002
Biobankrs559848002
1000 genomesrs559848002
hgdprs559848002
ensemblrs559848002
geneviewrs559848002
scholarrs559848002
googlers559848002
pharmgkbrs559848002
gwascentralrs559848002
openSNPrs559848002
23andMers559848002
23andMe allrs559848002
SNPshotrs559848002
SNPdbers559848002
MSV3drs559848002
GWAS Ctlgrs559848002
Max Magnitude0
ClinVar
Risk rs559848002(C;C) rs559848002(G;G)
Alt rs559848002(C;C) rs559848002(G;G)
Reference Rs559848002(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CDKN2A
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.21971146T>C
CLNSRC
CLNACC RCV000478806.1,