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rs2296212

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2296212(C;G)
Make rs2296212(G;G)
ReferenceGRCh37 37.1/132
Chromosome9
Position2191309
GeneSMARCA2
is asnp
is mentioned by
dbSNPrs2296212
ebirs2296212
HLIrs2296212
Exacrs2296212
Varsomers2296212
Maprs2296212
PheGenIrs2296212
hapmaprs2296212
1000 genomesrs2296212
hgdprs2296212
ensemblrs2296212
gopubmedrs2296212
geneviewrs2296212
scholarrs2296212
googlers2296212
pharmgkbrs2296212
gwascentralrs2296212
openSNPrs2296212
23andMers2296212
23andMe allrs2296212
SNP Nexus

SNPshotrs2296212
SNPdbers2296212
MSV3drs2296212
GWAS Ctlgrs2296212
GMAF0.1809
Max Magnitude0
? (C;C) (C;G) (G;G) 28
OMIM600014
DescSWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN,
Variant
Relatedalso


[PMID 19363039] Involvement of SMARCA2/BRM in the SWI/SNF chromatin-remodeling complex in schizophrenia.


GET Evidence
SMARCA2-D1546E
aa_change Asp1546Glu
aa_change_short D1546E
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.164622
summary



[PMID 23276717OA-icon.png] SWI/SNF gene variants and glioma risk and outcome.


ClinVar
Risk rs2296212(G;G)
Alt rs2296212(G;G)
Reference rs2296212(C;C)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene SMARCA2
CLNDBN not specified
Reversed 0
HGVS NC_000009.11:g.2191309C>G
CLNSRC ClinVar University of Chicago
CLNACC RCV000114292.2,