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rs763220502

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs763220502(A;A)
Make rs763220502(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position46726884
GeneSLC2A10
is asnp
is mentioned by
dbSNPrs763220502
ebirs763220502
HLIrs763220502
Exacrs763220502
Varsomers763220502
Maprs763220502
PheGenIrs763220502
hapmaprs763220502
1000 genomesrs763220502
hgdprs763220502
ensemblrs763220502
gopubmedrs763220502
geneviewrs763220502
scholarrs763220502
googlers763220502
pharmgkbrs763220502
gwascentralrs763220502
openSNPrs763220502
23andMers763220502
23andMe allrs763220502
SNP Nexus

SNPshotrs763220502
SNPdbers763220502
MSV3drs763220502
GWAS Ctlgrs763220502
Max Magnitude0
ClinVar
Risk rs763220502(A;A)
Alt rs763220502(A;A)
Reference rs763220502(G;G)
Significance Pathogenic
Disease Arterial tortuosity syndrome
Variation info
Gene SLC2A10
CLNDBN Arterial tortuosity syndrome
Reversed 0
HGVS NC_000020.10:g.45355523G>A
CLNSRC
CLNACC RCV000202526.1,