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rs796052550

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052550(A;A)
Make rs796052550(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position9798436
GeneGRIN2A, LOC105371077
is asnp
is mentioned by
dbSNPrs796052550
ebirs796052550
HLIrs796052550
Exacrs796052550
Varsomers796052550
Maprs796052550
PheGenIrs796052550
hapmaprs796052550
1000 genomesrs796052550
hgdprs796052550
ensemblrs796052550
gopubmedrs796052550
geneviewrs796052550
scholarrs796052550
googlers796052550
pharmgkbrs796052550
gwascentralrs796052550
openSNPrs796052550
23andMers796052550
23andMe allrs796052550
SNP Nexus

SNPshotrs796052550
SNPdbers796052550
MSV3drs796052550
GWAS Ctlgrs796052550
Max Magnitude0
ClinVar
Risk rs796052550(A;A)
Alt rs796052550(A;A)
Reference Rs796052550(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9892293C>T
CLNSRC
CLNACC RCV000187644.2,