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rs7194256

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs7194256(C;T)
Make rs7194256(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position55703779
GeneSLC6A2
is asnp
is mentioned by
dbSNPrs7194256
dbSNP (classic)rs7194256
ClinGenrs7194256
ebirs7194256
HLIrs7194256
Exacrs7194256
Gnomadrs7194256
Varsomers7194256
LitVarrs7194256
Maprs7194256
PheGenIrs7194256
Biobankrs7194256
1000 genomesrs7194256
hgdprs7194256
ensemblrs7194256
geneviewrs7194256
scholarrs7194256
googlers7194256
pharmgkbrs7194256
gwascentralrs7194256
openSNPrs7194256
23andMers7194256
SNPshotrs7194256
SNPdbers7194256
MSV3drs7194256
GWAS Ctlgrs7194256
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 27643232] ISH NIA OS-01 THE microRNA miR-19a-3p BINDS TO A POLYMORPHISM IN THE GENE FOR THE NORADRENALINE TRANSPORTER AND MAY INCREASE THE RISK OF CARDIOVASCULAR AND PSYCHIATRIC DISEASE.

[PMID 27753886] ISH NIA OS-01 THE microRNA miR-19a-3p BINDS TO A POLYMORPHISM IN THE GENE FOR THE NORADRENALINE TRANSPORTER AND MAY INCREASE THE RISK OF CARDIOVASCULAR AND PSYCHIATRIC DISEASE.


ClinVar
Risk rs7194256(T;T)
Alt rs7194256(T;T)
Reference Rs7194256(C;C)
Significance Probable-non-pathogenic
Disease Orthostatic intolerance
Variation info
Gene SLC6A2
CLNDBN Orthostatic intolerance
Reversed 0
HGVS NC_000016.9:g.55737691C>T
CLNSRC
CLNACC RCV000355154.1,