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rs796052582

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052582(G;T)
Make rs796052582(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position13608781
GeneGRIN2B, LOC105369668
is asnp
is mentioned by
dbSNPrs796052582
ebirs796052582
HLIrs796052582
Exacrs796052582
Varsomers796052582
Maprs796052582
PheGenIrs796052582
hapmaprs796052582
1000 genomesrs796052582
hgdprs796052582
ensemblrs796052582
gopubmedrs796052582
geneviewrs796052582
scholarrs796052582
googlers796052582
pharmgkbrs796052582
gwascentralrs796052582
openSNPrs796052582
23andMers796052582
23andMe allrs796052582
SNP Nexus

SNPshotrs796052582
SNPdbers796052582
MSV3drs796052582
GWAS Ctlgrs796052582
Max Magnitude0
ClinVar
Risk rs796052582(T;T)
Alt rs796052582(T;T)
Reference rs796052582(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13761715C>A
CLNSRC
CLNACC RCV000187718.1,