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rs1057517820

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517820(-;-)
Make rs1057517820(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position6703914
GeneSLC13A5
is asnp
is mentioned by
dbSNPrs1057517820
dbSNP (old)rs1057517820
ClinGenrs1057517820
ebirs1057517820
HLIrs1057517820
Exacrs1057517820
Gnomadrs1057517820
Varsomers1057517820
LitVarrs1057517820
Maprs1057517820
PheGenIrs1057517820
Biobankrs1057517820
1000 genomesrs1057517820
hgdprs1057517820
ensemblrs1057517820
gopubmedrs1057517820
geneviewrs1057517820
scholarrs1057517820
googlers1057517820
pharmgkbrs1057517820
gwascentralrs1057517820
openSNPrs1057517820
23andMers1057517820
23andMe allrs1057517820
SNPshotrs1057517820
SNPdbers1057517820
MSV3drs1057517820
GWAS Ctlgrs1057517820
Max Magnitude0
ClinVar
Risk rs1057517820(-;-)
Alt rs1057517820(-;-)
Reference Rs1057517820(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC13A5
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.6607233delC
CLNSRC
CLNACC RCV000413222.1,