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

rs966681982

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position6703140
GeneSLC13A5
is asnp
is mentioned by
dbSNPrs966681982
dbSNP (classic)rs966681982
ClinGenrs966681982
ebirs966681982
HLIrs966681982
Exacrs966681982
Gnomadrs966681982
Varsomers966681982
LitVarrs966681982
Maprs966681982
PheGenIrs966681982
Biobankrs966681982
1000 genomesrs966681982
hgdprs966681982
ensemblrs966681982
geneviewrs966681982
scholarrs966681982
googlers966681982
pharmgkbrs966681982
gwascentralrs966681982
openSNPrs966681982
23andMers966681982
SNPshotrs966681982
SNPdbers966681982
MSV3drs966681982
GWAS Ctlgrs966681982
Max Magnitude0
ClinVar
Risk rs966681982(C;C)
Alt rs966681982(C;C)
Reference Rs966681982(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.6606459T>C
CLNSRC
CLNACC RCV000485335.1,