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rs796052544

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052544(A;G)
Make rs796052544(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position9829500
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs796052544
ebirs796052544
HLIrs796052544
Exacrs796052544
Varsomers796052544
Maprs796052544
PheGenIrs796052544
hapmaprs796052544
1000 genomesrs796052544
hgdprs796052544
ensemblrs796052544
gopubmedrs796052544
geneviewrs796052544
scholarrs796052544
googlers796052544
pharmgkbrs796052544
gwascentralrs796052544
openSNPrs796052544
23andMers796052544
23andMe allrs796052544
SNP Nexus

SNPshotrs796052544
SNPdbers796052544
MSV3drs796052544
GWAS Ctlgrs796052544
Max Magnitude0
ClinVar
Risk rs796052544(G;G)
Alt rs796052544(G;G)
Reference rs796052544(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9923357T>C
CLNSRC
CLNACC RCV000187637.1,