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rs864309479

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309479(A;A)
Make rs864309479(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position46726987
GeneSLC2A10
is asnp
is mentioned by
dbSNPrs864309479
ebirs864309479
HLIrs864309479
Exacrs864309479
Varsomers864309479
Maprs864309479
PheGenIrs864309479
hapmaprs864309479
1000 genomesrs864309479
hgdprs864309479
ensemblrs864309479
gopubmedrs864309479
geneviewrs864309479
scholarrs864309479
googlers864309479
pharmgkbrs864309479
gwascentralrs864309479
openSNPrs864309479
23andMers864309479
23andMe allrs864309479
SNP Nexus

SNPshotrs864309479
SNPdbers864309479
MSV3drs864309479
GWAS Ctlgrs864309479
Max Magnitude0
ClinVar
Risk rs864309479(A;A)
Alt rs864309479(A;A)
Reference rs864309479(G;G)
Significance Pathogenic
Disease Arterial tortuosity syndrome
Variation info
Gene SLC2A10
CLNDBN Arterial tortuosity syndrome
Reversed 0
HGVS NC_000020.10:g.45355626G>A
CLNSRC
CLNACC RCV000202532.1,