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rs749426767

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs749426767(C;T)
Make rs749426767(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position42929215
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs749426767
dbSNP (classic)rs749426767
ClinGenrs749426767
ebirs749426767
HLIrs749426767
Exacrs749426767
Gnomadrs749426767
Varsomers749426767
LitVarrs749426767
Maprs749426767
PheGenIrs749426767
Biobankrs749426767
1000 genomesrs749426767
hgdprs749426767
ensemblrs749426767
geneviewrs749426767
scholarrs749426767
googlers749426767
pharmgkbrs749426767
gwascentralrs749426767
openSNPrs749426767
23andMers749426767
SNPshotrs749426767
SNPdbers749426767
MSV3drs749426767
GWAS Ctlgrs749426767
Max Magnitude0
ClinVar
Risk rs749426767(T;T)
Alt rs749426767(T;T)
Reference Rs749426767(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.43394886C>T
CLNSRC
CLNACC RCV000439467.1,