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rs61750174

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61750174(C;T)
Make rs61750174(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position8014704
GeneGUCY2D
is asnp
is mentioned by
dbSNPrs61750174
ebirs61750174
HLIrs61750174
Exacrs61750174
Varsomers61750174
Maprs61750174
PheGenIrs61750174
hapmaprs61750174
1000 genomesrs61750174
hgdprs61750174
ensemblrs61750174
gopubmedrs61750174
geneviewrs61750174
scholarrs61750174
googlers61750174
pharmgkbrs61750174
gwascentralrs61750174
openSNPrs61750174
23andMers61750174
23andMe allrs61750174
SNP Nexus

SNPshotrs61750174
SNPdbers61750174
MSV3drs61750174
GWAS Ctlgrs61750174
Max Magnitude0
OMIM600179
Desc
Variant0007
Relatedalso


ClinVar
Risk rs61750174(G,T;G,T)
Alt rs61750174(G,T;G,T)
Reference rs61750174(C;C)
Significance Pathogenic
Disease Cone-rod dystrophy 6 not provided
Variation info
Gene GUCY2D
CLNDBN Cone-rod dystrophy 6 not provided
Reversed 0
HGVS NC_000017.10:g.7918022C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009950.2, RCV000084864.1,