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rs752143706

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs752143706(C;T)
Make rs752143706(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position42927147
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs752143706
dbSNP (classic)rs752143706
ClinGenrs752143706
ebirs752143706
HLIrs752143706
Exacrs752143706
Gnomadrs752143706
Varsomers752143706
LitVarrs752143706
Maprs752143706
PheGenIrs752143706
Biobankrs752143706
1000 genomesrs752143706
hgdprs752143706
ensemblrs752143706
geneviewrs752143706
scholarrs752143706
googlers752143706
pharmgkbrs752143706
gwascentralrs752143706
openSNPrs752143706
23andMers752143706
SNPshotrs752143706
SNPdbers752143706
MSV3drs752143706
GWAS Ctlgrs752143706
Max Magnitude0
ClinVar
Risk rs752143706(T;T)
Alt rs752143706(T;T)
Reference Rs752143706(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.43392818C>T
CLNSRC
CLNACC RCV000440623.1,