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rs137957386

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137957386(A;A)
Make rs137957386(A;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position11027301
GeneMASP2
is asnp
is mentioned by
dbSNPrs137957386
ebirs137957386
HLIrs137957386
Exacrs137957386
Varsomers137957386
Maprs137957386
PheGenIrs137957386
hapmaprs137957386
1000 genomesrs137957386
hgdprs137957386
ensemblrs137957386
gopubmedrs137957386
geneviewrs137957386
scholarrs137957386
googlers137957386
pharmgkbrs137957386
gwascentralrs137957386
openSNPrs137957386
23andMers137957386
23andMe allrs137957386
SNP Nexus

SNPshotrs137957386
SNPdbers137957386
MSV3drs137957386
GWAS Ctlgrs137957386
Max Magnitude0

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

ClinVar
Risk rs137957386(A,C;A,C)
Alt rs137957386(A,C;A,C)
Reference rs137957386(T;T)
Significance Untested
Disease Malignant melanoma
Variation info
Gene MASP2
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000001.11:g.11027301T>A
CLNSRC ClinVar
CLNACC RCV000059831.2,