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

rs748547209

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs748547209(A;T)
Make rs748547209(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position56868327
GeneSLC12A3
is asnp
is mentioned by
dbSNPrs748547209
dbSNP (classic)rs748547209
ClinGenrs748547209
ebirs748547209
HLIrs748547209
Exacrs748547209
Gnomadrs748547209
Varsomers748547209
LitVarrs748547209
Maprs748547209
PheGenIrs748547209
Biobankrs748547209
1000 genomesrs748547209
hgdprs748547209
ensemblrs748547209
geneviewrs748547209
scholarrs748547209
googlers748547209
pharmgkbrs748547209
gwascentralrs748547209
openSNPrs748547209
23andMers748547209
23andMe allrs748547209
SNPshotrs748547209
SNPdbers748547209
MSV3drs748547209
GWAS Ctlgrs748547209
Max Magnitude0
ClinVar
Risk rs748547209(T;T)
Alt rs748547209(T;T)
Reference Rs748547209(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC12A3
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.56902239A>T
CLNSRC
CLNACC RCV000493117.1,