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rs796052549

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052549(A;A)
Make rs796052549(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position9798442
GeneGRIN2A, LOC105371077
is asnp
is mentioned by
dbSNPrs796052549
ebirs796052549
HLIrs796052549
Exacrs796052549
Varsomers796052549
Maprs796052549
PheGenIrs796052549
hapmaprs796052549
1000 genomesrs796052549
hgdprs796052549
ensemblrs796052549
gopubmedrs796052549
geneviewrs796052549
scholarrs796052549
googlers796052549
pharmgkbrs796052549
gwascentralrs796052549
openSNPrs796052549
23andMers796052549
23andMe allrs796052549
SNP Nexus

SNPshotrs796052549
SNPdbers796052549
MSV3drs796052549
GWAS Ctlgrs796052549
Max Magnitude0
ClinVar
Risk rs796052549(A;A)
Alt rs796052549(A;A)
Reference rs796052549(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9892299C>T
CLNSRC
CLNACC RCV000187643.2,