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rs370547023

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs370547023(C;T)
Make rs370547023(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position46726905
GeneSLC2A10
is asnp
is mentioned by
dbSNPrs370547023
ebirs370547023
HLIrs370547023
Exacrs370547023
Varsomers370547023
Maprs370547023
PheGenIrs370547023
hapmaprs370547023
1000 genomesrs370547023
hgdprs370547023
ensemblrs370547023
gopubmedrs370547023
geneviewrs370547023
scholarrs370547023
googlers370547023
pharmgkbrs370547023
gwascentralrs370547023
openSNPrs370547023
23andMers370547023
23andMe allrs370547023
SNP Nexus

SNPshotrs370547023
SNPdbers370547023
MSV3drs370547023
GWAS Ctlgrs370547023
Max Magnitude0
ClinVar
Risk rs370547023(T;T)
Alt rs370547023(T;T)
Reference rs370547023(C;C)
Significance Pathogenic
Disease Arterial tortuosity syndrome
Variation info
Gene SLC2A10
CLNDBN Arterial tortuosity syndrome
Reversed 0
HGVS NC_000020.10:g.45355544C>T
CLNSRC
CLNACC RCV000202558.1,