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rs753625117

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs753625117(C;C)
Make rs753625117(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position98396125
GeneCNGA3
is asnp
is mentioned by
dbSNPrs753625117
ebirs753625117
HLIrs753625117
Exacrs753625117
Varsomers753625117
Maprs753625117
PheGenIrs753625117
hapmaprs753625117
1000 genomesrs753625117
hgdprs753625117
ensemblrs753625117
gopubmedrs753625117
geneviewrs753625117
scholarrs753625117
googlers753625117
pharmgkbrs753625117
gwascentralrs753625117
openSNPrs753625117
23andMers753625117
23andMe allrs753625117
SNP Nexus

SNPshotrs753625117
SNPdbers753625117
MSV3drs753625117
GWAS Ctlgrs753625117
Max Magnitude0
ClinVar
Risk rs753625117(C;C)
Alt rs753625117(C;C)
Reference rs753625117(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CNGA3
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.99012588T>C
CLNSRC
CLNACC RCV000171300.1,