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rs139934930

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs139934930(C;T)
Make rs139934930(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position7827211
GenePER3
is asnp
is mentioned by
dbSNPrs139934930
ebirs139934930
HLIrs139934930
Exacrs139934930
Varsomers139934930
Maprs139934930
PheGenIrs139934930
hapmaprs139934930
1000 genomesrs139934930
hgdprs139934930
ensemblrs139934930
gopubmedrs139934930
geneviewrs139934930
scholarrs139934930
googlers139934930
pharmgkbrs139934930
gwascentralrs139934930
openSNPrs139934930
23andMers139934930
23andMe allrs139934930
SNP Nexus

SNPshotrs139934930
SNPdbers139934930
MSV3drs139934930
GWAS Ctlgrs139934930
Max Magnitude0

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

ClinVar
Risk rs139934930(T;T)
Alt rs139934930(T;T)
Reference rs139934930(C;C)
Significance Untested
Disease Malignant melanoma
Variation info
Gene PER3
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000001.11:g.7827211C>T
CLNSRC ClinVar
CLNACC RCV000060248.2,