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rs767864243

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs767864243(C;T)
Make rs767864243(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position46725349
GeneSLC2A10
is asnp
is mentioned by
dbSNPrs767864243
ebirs767864243
HLIrs767864243
Exacrs767864243
Varsomers767864243
Maprs767864243
PheGenIrs767864243
hapmaprs767864243
1000 genomesrs767864243
hgdprs767864243
ensemblrs767864243
gopubmedrs767864243
geneviewrs767864243
scholarrs767864243
googlers767864243
pharmgkbrs767864243
gwascentralrs767864243
openSNPrs767864243
23andMers767864243
23andMe allrs767864243
SNP Nexus

SNPshotrs767864243
SNPdbers767864243
MSV3drs767864243
GWAS Ctlgrs767864243
Max Magnitude0
ClinVar
Risk rs767864243(T;T)
Alt rs767864243(T;T)
Reference rs767864243(C;C)
Significance Pathogenic
Disease not provided Arterial tortuosity syndrome not specified
Variation info
Gene SLC2A10
CLNDBN not provided Arterial tortuosity syndrome not specified
Reversed 0
HGVS NC_000020.10:g.45353988C>T
CLNSRC
CLNACC RCV000197165.1, RCV000202447.1, RCV000202814.1,