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rs796052578

From SNPedia

Orientationminus
Make rs796052578(-;-)
Make rs796052578(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position13567034
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs796052578
ebirs796052578
HLIrs796052578
Exacrs796052578
Varsomers796052578
Maprs796052578
PheGenIrs796052578
hapmaprs796052578
1000 genomesrs796052578
hgdprs796052578
ensemblrs796052578
gopubmedrs796052578
geneviewrs796052578
scholarrs796052578
googlers796052578
pharmgkbrs796052578
gwascentralrs796052578
openSNPrs796052578
23andMers796052578
23andMe allrs796052578
SNP Nexus

SNPshotrs796052578
SNPdbers796052578
MSV3drs796052578
GWAS Ctlgrs796052578
Max Magnitude
ClinVar
Risk rs796052578(;)
Alt rs796052578(;)
Reference rs796052578(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13719968delG
CLNSRC
CLNACC RCV000187708.2,