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rs761721442

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs761721442(A;A)
Make rs761721442(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position46726988
GeneSLC2A10
is asnp
is mentioned by
dbSNPrs761721442
ebirs761721442
HLIrs761721442
Exacrs761721442
Varsomers761721442
Maprs761721442
PheGenIrs761721442
hapmaprs761721442
1000 genomesrs761721442
hgdprs761721442
ensemblrs761721442
gopubmedrs761721442
geneviewrs761721442
scholarrs761721442
googlers761721442
pharmgkbrs761721442
gwascentralrs761721442
openSNPrs761721442
23andMers761721442
23andMe allrs761721442
SNP Nexus

SNPshotrs761721442
SNPdbers761721442
MSV3drs761721442
GWAS Ctlgrs761721442
Max Magnitude0
ClinVar
Risk rs761721442(A;A)
Alt rs761721442(A;A)
Reference rs761721442(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC2A10
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.45355627T>A
CLNSRC
CLNACC RCV000197685.1,