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

rs541299023

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs541299023(A;A)
Make rs541299023(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position8013951
GeneGUCY2D
is asnp
is mentioned by
dbSNPrs541299023
dbSNP (classic)rs541299023
ClinGenrs541299023
ebirs541299023
HLIrs541299023
Exacrs541299023
Gnomadrs541299023
Varsomers541299023
LitVarrs541299023
Maprs541299023
PheGenIrs541299023
Biobankrs541299023
1000 genomesrs541299023
hgdprs541299023
ensemblrs541299023
geneviewrs541299023
scholarrs541299023
googlers541299023
pharmgkbrs541299023
gwascentralrs541299023
openSNPrs541299023
23andMers541299023
23andMe allrs541299023
SNPshotrs541299023
SNPdbers541299023
MSV3drs541299023
GWAS Ctlgrs541299023
Max Magnitude0
ClinVar
Risk rs541299023(A;A) rs541299023(T;T)
Alt rs541299023(A;A) rs541299023(T;T)
Reference Rs541299023(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GUCY2D
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7917269G>T
CLNSRC
CLNACC RCV000478042.1,