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

rs145734330

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs145734330(A;A)
Make rs145734330(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position15930681
GeneSPEN
is asnp
is mentioned by
dbSNPrs145734330
ebirs145734330
HLIrs145734330
Exacrs145734330
Varsomers145734330
Maprs145734330
PheGenIrs145734330
hapmaprs145734330
1000 genomesrs145734330
hgdprs145734330
ensemblrs145734330
gopubmedrs145734330
geneviewrs145734330
scholarrs145734330
googlers145734330
pharmgkbrs145734330
gwascentralrs145734330
openSNPrs145734330
23andMers145734330
23andMe allrs145734330
SNP Nexus

SNPshotrs145734330
SNPdbers145734330
MSV3drs145734330
GWAS Ctlgrs145734330
Max Magnitude0

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

ClinVar
Risk rs145734330(A;A)
Alt rs145734330(A;A)
Reference rs145734330(G;G)
Significance Untested
Disease Malignant melanoma
Variation info
Gene SPEN
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000001.11:g.15930681G>A
CLNSRC ClinVar
CLNACC RCV000059971.2,