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rs1057524391

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524391(C;T)
Make rs1057524391(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position45850995
GeneARID2, LOC105369745
is asnp
is mentioned by
dbSNPrs1057524391
dbSNP (old)rs1057524391
ClinGenrs1057524391
ebirs1057524391
HLIrs1057524391
Exacrs1057524391
Gnomadrs1057524391
Varsomers1057524391
LitVarrs1057524391
Maprs1057524391
PheGenIrs1057524391
Biobankrs1057524391
1000 genomesrs1057524391
hgdprs1057524391
ensemblrs1057524391
gopubmedrs1057524391
geneviewrs1057524391
scholarrs1057524391
googlers1057524391
pharmgkbrs1057524391
gwascentralrs1057524391
openSNPrs1057524391
23andMers1057524391
23andMe allrs1057524391
SNPshotrs1057524391
SNPdbers1057524391
MSV3drs1057524391
GWAS Ctlgrs1057524391
Max Magnitude0
ClinVar
Risk rs1057524391(T;T)
Alt rs1057524391(T;T)
Reference Rs1057524391(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ARID2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.46244778C>T
CLNSRC
CLNACC RCV000438912.1,