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

rs776095655

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs776095655(A;A)
Make rs776095655(A;C)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position42927684
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs776095655
dbSNP (classic)rs776095655
ClinGenrs776095655
ebirs776095655
HLIrs776095655
Exacrs776095655
Gnomadrs776095655
Varsomers776095655
LitVarrs776095655
Maprs776095655
PheGenIrs776095655
Biobankrs776095655
1000 genomesrs776095655
hgdprs776095655
ensemblrs776095655
geneviewrs776095655
scholarrs776095655
googlers776095655
pharmgkbrs776095655
gwascentralrs776095655
openSNPrs776095655
23andMers776095655
SNPshotrs776095655
SNPdbers776095655
MSV3drs776095655
GWAS Ctlgrs776095655
Max Magnitude0
ClinVar
Risk rs776095655(A;A) rs776095655(T;T)
Alt rs776095655(A;A) rs776095655(T;T)
Reference Rs776095655(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.43393355C>T
CLNSRC
CLNACC RCV000364606.1,