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rs145449783

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs145449783(A;A)
Make rs145449783(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position6529168
GeneNOL9
is asnp
is mentioned by
dbSNPrs145449783
ebirs145449783
HLIrs145449783
Exacrs145449783
Varsomers145449783
Maprs145449783
PheGenIrs145449783
hapmaprs145449783
1000 genomesrs145449783
hgdprs145449783
ensemblrs145449783
gopubmedrs145449783
geneviewrs145449783
scholarrs145449783
googlers145449783
pharmgkbrs145449783
gwascentralrs145449783
openSNPrs145449783
23andMers145449783
23andMe allrs145449783
SNP Nexus

SNPshotrs145449783
SNPdbers145449783
MSV3drs145449783
GWAS Ctlgrs145449783
Max Magnitude0
ClinVar
Risk rs145449783(A;A)
Alt rs145449783(A;A)
Reference rs145449783(G;G)
Significance Untested
Disease Malignant melanoma
Variation info
Gene NOL9
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000001.11:g.6529168G>A
CLNSRC ClinVar
CLNACC RCV000060234.2,


[PMID 21499247OA-icon.png] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.