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

rs796052562

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052562(A;A)
Make rs796052562(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position9829506
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs796052562
ebirs796052562
HLIrs796052562
Exacrs796052562
Varsomers796052562
Maprs796052562
PheGenIrs796052562
hapmaprs796052562
1000 genomesrs796052562
hgdprs796052562
ensemblrs796052562
gopubmedrs796052562
geneviewrs796052562
scholarrs796052562
googlers796052562
pharmgkbrs796052562
gwascentralrs796052562
openSNPrs796052562
23andMers796052562
23andMe allrs796052562
SNP Nexus

SNPshotrs796052562
SNPdbers796052562
MSV3drs796052562
GWAS Ctlgrs796052562
Max Magnitude0
ClinVar
Risk rs796052562(A;A)
Alt rs796052562(A;A)
Reference rs796052562(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9923363G>T
CLNSRC
CLNACC RCV000187675.1,