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rs2230307

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2230307(A;A)
Make rs2230307(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position99896369
GeneAGL
is asnp
is mentioned by
dbSNPrs2230307
dbSNP (old)rs2230307
ClinGenrs2230307
ebirs2230307
HLIrs2230307
Exacrs2230307
Gnomadrs2230307
Varsomers2230307
Maprs2230307
PheGenIrs2230307
Biobankrs2230307
1000 genomesrs2230307
hgdprs2230307
ensemblrs2230307
gopubmedrs2230307
geneviewrs2230307
scholarrs2230307
googlers2230307
pharmgkbrs2230307
gwascentralrs2230307
openSNPrs2230307
23andMers2230307
23andMe allrs2230307
SNP Nexus

SNPshotrs2230307
SNPdbers2230307
MSV3drs2230307
GWAS Ctlgrs2230307
Max Magnitude0

[PMID 26343869] Genome-wide association study on progression of carotid artery intima media thickness over 10 years in a Chinese cohort.

ClinVar
Risk rs2230307(A;A)
Alt rs2230307(A;A)
Reference Rs2230307(G;G)
Significance Probable-non-pathogenic
Disease not specified Glycogen storage disease type III
Variation info
Gene AGL
CLNDBN not specified Glycogen storage disease type III
Reversed 0
HGVS NC_000001.10:g.100361925G>A
CLNSRC
CLNACC RCV000247829.2, RCV000324145.1,