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rs200247956

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200247956(A;A)
Make rs200247956(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position42929655
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs200247956
ebirs200247956
HLIrs200247956
Exacrs200247956
Varsomers200247956
Maprs200247956
PheGenIrs200247956
hapmaprs200247956
1000 genomesrs200247956
hgdprs200247956
ensemblrs200247956
gopubmedrs200247956
geneviewrs200247956
scholarrs200247956
googlers200247956
pharmgkbrs200247956
gwascentralrs200247956
openSNPrs200247956
23andMers200247956
23andMe allrs200247956
SNP Nexus

SNPshotrs200247956
SNPdbers200247956
MSV3drs200247956
GWAS Ctlgrs200247956
Max Magnitude0
ClinVar
Risk rs200247956(A;A)
Alt rs200247956(A;A)
Reference rs200247956(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.43395326G>A
CLNSRC
CLNACC RCV000189396.1,