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

rs572620317

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs572620317(C;C)
Make rs572620317(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position46725453
GeneSLC2A10
is asnp
is mentioned by
dbSNPrs572620317
ebirs572620317
HLIrs572620317
Exacrs572620317
Varsomers572620317
Maprs572620317
PheGenIrs572620317
hapmaprs572620317
1000 genomesrs572620317
hgdprs572620317
ensemblrs572620317
gopubmedrs572620317
geneviewrs572620317
scholarrs572620317
googlers572620317
pharmgkbrs572620317
gwascentralrs572620317
openSNPrs572620317
23andMers572620317
23andMe allrs572620317
SNP Nexus

SNPshotrs572620317
SNPdbers572620317
MSV3drs572620317
GWAS Ctlgrs572620317
Max Magnitude0
ClinVar
Risk rs572620317(A,C;A,C)
Alt rs572620317(A,C;A,C)
Reference rs572620317(T;T)
Significance Pathogenic
Disease Arterial tortuosity syndrome
Variation info
Gene SLC2A10
CLNDBN Arterial tortuosity syndrome
Reversed 0
HGVS NC_000020.10:g.45354092T>A
CLNSRC
CLNACC RCV000202463.1,