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rs121918126

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918126(C;C)
Make rs121918126(C;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position55698005
GeneSLC6A2
is asnp
is mentioned by
dbSNPrs121918126
ebirs121918126
HLIrs121918126
Exacrs121918126
Varsomers121918126
Maprs121918126
PheGenIrs121918126
hapmaprs121918126
1000 genomesrs121918126
hgdprs121918126
ensemblrs121918126
gopubmedrs121918126
geneviewrs121918126
scholarrs121918126
googlers121918126
pharmgkbrs121918126
gwascentralrs121918126
openSNPrs121918126
23andMers121918126
23andMe allrs121918126
SNP Nexus

SNPshotrs121918126
SNPdbers121918126
MSV3drs121918126
GWAS Ctlgrs121918126
Max Magnitude0
OMIM163970
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918126(A,C,T;A,C,T)
Alt rs121918126(A,C,T;A,C,T)
Reference rs121918126(G;G)
Significance Pathogenic
Disease Orthostatic intolerance
Variation info
Gene SLC6A2
CLNDBN Orthostatic intolerance
Reversed 0
HGVS NC_000016.9:g.55731917G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000015043.25,