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rs796052241

From SNPedia

Orientationplus
Make rs796052241(-;-)
Make rs796052241(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position45852564
GeneARID2
is asnp
is mentioned by
dbSNPrs796052241
ebirs796052241
HLIrs796052241
Exacrs796052241
Varsomers796052241
Maprs796052241
PheGenIrs796052241
hapmaprs796052241
1000 genomesrs796052241
hgdprs796052241
ensemblrs796052241
gopubmedrs796052241
geneviewrs796052241
scholarrs796052241
googlers796052241
pharmgkbrs796052241
gwascentralrs796052241
openSNPrs796052241
23andMers796052241
23andMe allrs796052241
SNP Nexus

SNPshotrs796052241
SNPdbers796052241
MSV3drs796052241
GWAS Ctlgrs796052241
Max Magnitude
ClinVar
Risk rs796052241(;)
Alt rs796052241(;)
Reference rs796052241(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ARID2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.46246347delC
CLNSRC
CLNACC RCV000190119.1,