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rs753723351

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs753723351(A;A)
Make rs753723351(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position46726909
GeneSLC2A10
is asnp
is mentioned by
dbSNPrs753723351
ebirs753723351
HLIrs753723351
Exacrs753723351
Varsomers753723351
Maprs753723351
PheGenIrs753723351
hapmaprs753723351
1000 genomesrs753723351
hgdprs753723351
ensemblrs753723351
gopubmedrs753723351
geneviewrs753723351
scholarrs753723351
googlers753723351
pharmgkbrs753723351
gwascentralrs753723351
openSNPrs753723351
23andMers753723351
23andMe allrs753723351
SNP Nexus

SNPshotrs753723351
SNPdbers753723351
MSV3drs753723351
GWAS Ctlgrs753723351
Max Magnitude0
ClinVar
Risk rs753723351(A;A)
Alt rs753723351(A;A)
Reference rs753723351(G;G)
Significance Pathogenic
Disease Arterial tortuosity syndrome
Variation info
Gene SLC2A10
CLNDBN Arterial tortuosity syndrome
Reversed 0
HGVS NC_000020.10:g.45355548G>A
CLNSRC
CLNACC RCV000202473.1,