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

rs141882357

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs141882357(A;A)
Make rs141882357(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position12746532
GeneC1orf158
is asnp
is mentioned by
dbSNPrs141882357
ebirs141882357
HLIrs141882357
Exacrs141882357
Varsomers141882357
Maprs141882357
PheGenIrs141882357
hapmaprs141882357
1000 genomesrs141882357
hgdprs141882357
ensemblrs141882357
gopubmedrs141882357
geneviewrs141882357
scholarrs141882357
googlers141882357
pharmgkbrs141882357
gwascentralrs141882357
openSNPrs141882357
23andMers141882357
23andMe allrs141882357
SNP Nexus

SNPshotrs141882357
SNPdbers141882357
MSV3drs141882357
GWAS Ctlgrs141882357
Max Magnitude0
ClinVar
Risk rs141882357(A;A)
Alt rs141882357(A;A)
Reference rs141882357(G;G)
Significance Untested
Disease Malignant melanoma
Variation info
Gene C1orf158
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000001.11:g.12746532G>A
CLNSRC ClinVar
CLNACC RCV000059858.2,


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