Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs201439880

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201439880(A;A)
Make rs201439880(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position13564226
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs201439880
dbSNP (old)rs201439880
ClinGenrs201439880
ebirs201439880
HLIrs201439880
Exacrs201439880
Gnomadrs201439880
Varsomers201439880
Maprs201439880
PheGenIrs201439880
Biobankrs201439880
1000 genomesrs201439880
hgdprs201439880
ensemblrs201439880
gopubmedrs201439880
geneviewrs201439880
scholarrs201439880
googlers201439880
pharmgkbrs201439880
gwascentralrs201439880
openSNPrs201439880
23andMers201439880
23andMe allrs201439880
SNPshotrs201439880
SNPdbers201439880
MSV3drs201439880
GWAS Ctlgrs201439880
Max Magnitude0
ClinVar
Risk rs201439880(A;A) rs201439880(C;C)
Alt rs201439880(A;A) rs201439880(C;C)
Reference Rs201439880(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.13717160G>C
CLNSRC
CLNACC RCV000353647.1,