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rs1057524392

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524392(A;T)
Make rs1057524392(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position13615621
GeneGRIN2B, LOC105369668
is asnp
is mentioned by
dbSNPrs1057524392
dbSNP (old)rs1057524392
ClinGenrs1057524392
ebirs1057524392
HLIrs1057524392
Exacrs1057524392
Gnomadrs1057524392
Varsomers1057524392
LitVarrs1057524392
Maprs1057524392
PheGenIrs1057524392
Biobankrs1057524392
1000 genomesrs1057524392
hgdprs1057524392
ensemblrs1057524392
gopubmedrs1057524392
geneviewrs1057524392
scholarrs1057524392
googlers1057524392
pharmgkbrs1057524392
gwascentralrs1057524392
openSNPrs1057524392
23andMers1057524392
23andMe allrs1057524392
SNPshotrs1057524392
SNPdbers1057524392
MSV3drs1057524392
GWAS Ctlgrs1057524392
Max Magnitude0
ClinVar
Risk rs1057524392(T;T)
Alt rs1057524392(T;T)
Reference Rs1057524392(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13768555T>A
CLNSRC
CLNACC RCV000422130.1,