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rs786205500

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205500(C;C)
Make rs786205500(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position8003574
GeneGUCY2D
is asnp
is mentioned by
dbSNPrs786205500
ebirs786205500
HLIrs786205500
Exacrs786205500
Varsomers786205500
Maprs786205500
PheGenIrs786205500
hapmaprs786205500
1000 genomesrs786205500
hgdprs786205500
ensemblrs786205500
gopubmedrs786205500
geneviewrs786205500
scholarrs786205500
googlers786205500
pharmgkbrs786205500
gwascentralrs786205500
openSNPrs786205500
23andMers786205500
23andMe allrs786205500
SNP Nexus

SNPshotrs786205500
SNPdbers786205500
MSV3drs786205500
GWAS Ctlgrs786205500
Max Magnitude0
ClinVar
Risk rs786205500(C;C)
Alt rs786205500(C;C)
Reference rs786205500(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GUCY2D
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7906892T>C
CLNSRC
CLNACC RCV000171250.1,