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rs146579504

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs146579504(C;T)
Make rs146579504(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position46725727
GeneSLC2A10
is asnp
is mentioned by
dbSNPrs146579504
ebirs146579504
HLIrs146579504
Exacrs146579504
Varsomers146579504
Maprs146579504
PheGenIrs146579504
hapmaprs146579504
1000 genomesrs146579504
hgdprs146579504
ensemblrs146579504
gopubmedrs146579504
geneviewrs146579504
scholarrs146579504
googlers146579504
pharmgkbrs146579504
gwascentralrs146579504
openSNPrs146579504
23andMers146579504
23andMe allrs146579504
SNP Nexus

SNPshotrs146579504
SNPdbers146579504
MSV3drs146579504
GWAS Ctlgrs146579504
Max Magnitude0
ClinVar
Risk rs146579504(T;T)
Alt rs146579504(T;T)
Reference rs146579504(C;C)
Significance Pathogenic
Disease not provided Arterial tortuosity syndrome
Variation info
Gene SLC2A10
CLNDBN not provided Arterial tortuosity syndrome
Reversed 0
HGVS NC_000020.10:g.45354366C>T
CLNSRC
CLNACC RCV000195605.1, RCV000202453.1,