Have questions? Visit https://www.reddit.com/r/SNPedia

rs13306668

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs13306668(A;A)
Make rs13306668(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position56879088
GeneSLC12A3
is asnp
is mentioned by
dbSNPrs13306668
dbSNP (classic)rs13306668
ClinGenrs13306668
ebirs13306668
HLIrs13306668
Exacrs13306668
Gnomadrs13306668
Varsomers13306668
LitVarrs13306668
Maprs13306668
PheGenIrs13306668
Biobankrs13306668
1000 genomesrs13306668
hgdprs13306668
ensemblrs13306668
geneviewrs13306668
scholarrs13306668
googlers13306668
pharmgkbrs13306668
gwascentralrs13306668
openSNPrs13306668
23andMers13306668
23andMe allrs13306668
SNPshotrs13306668
SNPdbers13306668
MSV3drs13306668
GWAS Ctlgrs13306668
Max Magnitude0
? (A;A) (A;G) (G;G) 28


ClinVar
Risk rs13306668(A;A) rs13306668(C;C) rs13306668(T;T)
Alt rs13306668(A;A) rs13306668(C;C) rs13306668(T;T)
Reference Rs13306668(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC12A3
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.56913000G>T
CLNSRC
CLNACC RCV000439274.1,