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rs756457861

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs756457861(C;T)
Make rs756457861(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position46725721
GeneSLC2A10
is asnp
is mentioned by
dbSNPrs756457861
ebirs756457861
HLIrs756457861
Exacrs756457861
Varsomers756457861
Maprs756457861
PheGenIrs756457861
hapmaprs756457861
1000 genomesrs756457861
hgdprs756457861
ensemblrs756457861
gopubmedrs756457861
geneviewrs756457861
scholarrs756457861
googlers756457861
pharmgkbrs756457861
gwascentralrs756457861
openSNPrs756457861
23andMers756457861
23andMe allrs756457861
SNP Nexus

SNPshotrs756457861
SNPdbers756457861
MSV3drs756457861
GWAS Ctlgrs756457861
Max Magnitude0
ClinVar
Risk rs756457861(A,T;A,T)
Alt rs756457861(A,T;A,T)
Reference rs756457861(C;C)
Significance Pathogenic
Disease Arterial tortuosity syndrome
Variation info
Gene SLC2A10
CLNDBN Arterial tortuosity syndrome
Reversed 0
HGVS NC_000020.10:g.45354360C>T
CLNSRC
CLNACC RCV000202510.1,