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rs1057518299

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518299(-;C)
Make rs1057518299(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position6693091
GeneSLC13A5
is asnp
is mentioned by
dbSNPrs1057518299
dbSNP (old)rs1057518299
ClinGenrs1057518299
ebirs1057518299
HLIrs1057518299
Exacrs1057518299
Gnomadrs1057518299
Varsomers1057518299
LitVarrs1057518299
Maprs1057518299
PheGenIrs1057518299
Biobankrs1057518299
1000 genomesrs1057518299
hgdprs1057518299
ensemblrs1057518299
gopubmedrs1057518299
geneviewrs1057518299
scholarrs1057518299
googlers1057518299
pharmgkbrs1057518299
gwascentralrs1057518299
openSNPrs1057518299
23andMers1057518299
23andMe allrs1057518299
SNPshotrs1057518299
SNPdbers1057518299
MSV3drs1057518299
GWAS Ctlgrs1057518299
Max Magnitude0
ClinVar
Risk rs1057518299(C;C)
Alt rs1057518299(C;C)
Reference Rs1057518299(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC13A5
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.6596411dupG
CLNSRC
CLNACC RCV000414557.1,