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rs796052560

From SNPedia

Orientationminus
Make rs796052560(-;-)
Make rs796052560(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position9938339
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs796052560
ebirs796052560
HLIrs796052560
Exacrs796052560
Varsomers796052560
Maprs796052560
PheGenIrs796052560
hapmaprs796052560
1000 genomesrs796052560
hgdprs796052560
ensemblrs796052560
gopubmedrs796052560
geneviewrs796052560
scholarrs796052560
googlers796052560
pharmgkbrs796052560
gwascentralrs796052560
openSNPrs796052560
23andMers796052560
23andMe allrs796052560
SNP Nexus

SNPshotrs796052560
SNPdbers796052560
MSV3drs796052560
GWAS Ctlgrs796052560
Max Magnitude
ClinVar
Risk rs796052560(;)
Alt rs796052560(;)
Reference rs796052560(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.10032196delG
CLNSRC
CLNACC RCV000187672.1,