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rs797045015

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797045015(A;G)
Make rs797045015(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position10180098
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs797045015
ebirs797045015
HLIrs797045015
Exacrs797045015
Varsomers797045015
Maprs797045015
PheGenIrs797045015
hapmaprs797045015
1000 genomesrs797045015
hgdprs797045015
ensemblrs797045015
gopubmedrs797045015
geneviewrs797045015
scholarrs797045015
googlers797045015
pharmgkbrs797045015
gwascentralrs797045015
openSNPrs797045015
23andMers797045015
23andMe allrs797045015
SNP Nexus

SNPshotrs797045015
SNPdbers797045015
MSV3drs797045015
GWAS Ctlgrs797045015
Max Magnitude0
ClinVar
Risk rs797045015(G;G)
Alt rs797045015(G;G)
Reference rs797045015(A;A)
Significance Probable-non-pathogenic
Disease Epilepsy
Variation info
Gene GRIN2A
CLNDBN Epilepsy, focal, with speech disorder and with or without mental retardation
Reversed 1
HGVS NC_000016.9:g.10273955T>C
CLNSRC
CLNACC RCV000190515.2,