Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052242

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052242(A;A)
Make rs796052242(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position45837325
GeneARID2, LOC105369745
is asnp
is mentioned by
dbSNPrs796052242
ebirs796052242
HLIrs796052242
Exacrs796052242
Varsomers796052242
Maprs796052242
PheGenIrs796052242
hapmaprs796052242
1000 genomesrs796052242
hgdprs796052242
ensemblrs796052242
gopubmedrs796052242
geneviewrs796052242
scholarrs796052242
googlers796052242
pharmgkbrs796052242
gwascentralrs796052242
openSNPrs796052242
23andMers796052242
23andMe allrs796052242
SNP Nexus

SNPshotrs796052242
SNPdbers796052242
MSV3drs796052242
GWAS Ctlgrs796052242
Max Magnitude0
ClinVar
Risk rs796052242(A;A)
Alt rs796052242(A;A)
Reference rs796052242(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene ARID2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.46231108T>A
CLNSRC
CLNACC RCV000190120.2,