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rs772995852

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs772995852(C;G)
Make rs772995852(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position45852441
GeneARID2
is asnp
is mentioned by
dbSNPrs772995852
ebirs772995852
HLIrs772995852
Exacrs772995852
Varsomers772995852
Maprs772995852
PheGenIrs772995852
hapmaprs772995852
1000 genomesrs772995852
hgdprs772995852
ensemblrs772995852
gopubmedrs772995852
geneviewrs772995852
scholarrs772995852
googlers772995852
pharmgkbrs772995852
gwascentralrs772995852
openSNPrs772995852
23andMers772995852
23andMe allrs772995852
SNP Nexus

SNPshotrs772995852
SNPdbers772995852
MSV3drs772995852
GWAS Ctlgrs772995852
Max Magnitude0
ClinVar
Risk rs772995852(G;G)
Alt rs772995852(G;G)
Reference rs772995852(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ARID2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.46246224C>T
CLNSRC
CLNACC RCV000190117.2,