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rs587776600

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776600(-;-)
Make rs587776600(-;G)
ReferenceGRCh38 38.1/142
Chromosome20
Position46726909
GeneSLC2A10
is asnp
is mentioned by
dbSNPrs587776600
ebirs587776600
HLIrs587776600
Exacrs587776600
Varsomers587776600
Maprs587776600
PheGenIrs587776600
hapmaprs587776600
1000 genomesrs587776600
hgdprs587776600
ensemblrs587776600
gopubmedrs587776600
geneviewrs587776600
scholarrs587776600
googlers587776600
pharmgkbrs587776600
gwascentralrs587776600
openSNPrs587776600
23andMers587776600
23andMe allrs587776600
SNP Nexus

SNPshotrs587776600
SNPdbers587776600
MSV3drs587776600
GWAS Ctlgrs587776600
Max Magnitude0
ClinVar
Risk rs587776600(;)
Alt rs587776600(;)
Reference rs587776600(G;G)
Significance Pathogenic
Disease Arterial tortuosity syndrome not provided
Variation info
Gene SLC2A10
CLNDBN Arterial tortuosity syndrome not provided
Reversed 0
HGVS NC_000020.10:g.45355548delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000004849.3, RCV000197366.1,