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rs796052240

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052240(-;-)
Make rs796052240(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position45850659
GeneARID2, LOC105369745
is asnp
is mentioned by
dbSNPrs796052240
dbSNP (old)rs796052240
ClinGenrs796052240
ebirs796052240
HLIrs796052240
Exacrs796052240
Varsomers796052240
Maprs796052240
PheGenIrs796052240
Biobankrs796052240
1000 genomesrs796052240
hgdprs796052240
ensemblrs796052240
gopubmedrs796052240
geneviewrs796052240
scholarrs796052240
googlers796052240
pharmgkbrs796052240
gwascentralrs796052240
openSNPrs796052240
23andMers796052240
23andMe allrs796052240
SNP Nexus

SNPshotrs796052240
SNPdbers796052240
MSV3drs796052240
GWAS Ctlgrs796052240
Max Magnitude0
ClinVar
Risk rs796052240(-;-)
Alt rs796052240(-;-)
Reference Rs796052240(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ARID2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.46244442delG
CLNSRC
CLNACC RCV000190118.3,