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rs786205499

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205499(C;C)
Make rs786205499(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position8003463
GeneGUCY2D
is asnp
is mentioned by
dbSNPrs786205499
ebirs786205499
HLIrs786205499
Exacrs786205499
Varsomers786205499
Maprs786205499
PheGenIrs786205499
hapmaprs786205499
1000 genomesrs786205499
hgdprs786205499
ensemblrs786205499
gopubmedrs786205499
geneviewrs786205499
scholarrs786205499
googlers786205499
pharmgkbrs786205499
gwascentralrs786205499
openSNPrs786205499
23andMers786205499
23andMe allrs786205499
SNP Nexus

SNPshotrs786205499
SNPdbers786205499
MSV3drs786205499
GWAS Ctlgrs786205499
Max Magnitude0
ClinVar
Risk rs786205499(C;C)
Alt rs786205499(C;C)
Reference rs786205499(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GUCY2D
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7906781T>C
CLNSRC
CLNACC RCV000171249.1,