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rs1057518298

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518298(A;A)
Make rs1057518298(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position6702965
GeneSLC13A5
is asnp
is mentioned by
dbSNPrs1057518298
dbSNP (old)rs1057518298
ClinGenrs1057518298
ebirs1057518298
HLIrs1057518298
Exacrs1057518298
Gnomadrs1057518298
Varsomers1057518298
LitVarrs1057518298
Maprs1057518298
PheGenIrs1057518298
Biobankrs1057518298
1000 genomesrs1057518298
hgdprs1057518298
ensemblrs1057518298
gopubmedrs1057518298
geneviewrs1057518298
scholarrs1057518298
googlers1057518298
pharmgkbrs1057518298
gwascentralrs1057518298
openSNPrs1057518298
23andMers1057518298
23andMe allrs1057518298
SNPshotrs1057518298
SNPdbers1057518298
MSV3drs1057518298
GWAS Ctlgrs1057518298
Max Magnitude0
ClinVar
Risk rs1057518298(A;A)
Alt rs1057518298(A;A)
Reference Rs1057518298(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC13A5
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.6606284C>T
CLNSRC
CLNACC RCV000413948.1,