Have questions? Visit https://www.reddit.com/r/SNPedia

rs771386274

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs771386274(C;T)
Make rs771386274(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position42929868
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs771386274
dbSNP (classic)rs771386274
ClinGenrs771386274
ebirs771386274
HLIrs771386274
Exacrs771386274
Gnomadrs771386274
Varsomers771386274
LitVarrs771386274
Maprs771386274
PheGenIrs771386274
Biobankrs771386274
1000 genomesrs771386274
hgdprs771386274
ensemblrs771386274
geneviewrs771386274
scholarrs771386274
googlers771386274
pharmgkbrs771386274
gwascentralrs771386274
openSNPrs771386274
23andMers771386274
SNPshotrs771386274
SNPdbers771386274
MSV3drs771386274
GWAS Ctlgrs771386274
Max Magnitude0
ClinVar
Risk rs771386274(A;A) rs771386274(T;T)
Alt rs771386274(A;A) rs771386274(T;T)
Reference Rs771386274(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.43395539C>A
CLNSRC
CLNACC RCV000254738.1,