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rs1057517028

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517028(A;A)
Make rs1057517028(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position73635381
GeneSLC17A5
is asnp
is mentioned by
dbSNPrs1057517028
dbSNP (classic)rs1057517028
ClinGenrs1057517028
ebirs1057517028
HLIrs1057517028
Exacrs1057517028
Gnomadrs1057517028
Varsomers1057517028
LitVarrs1057517028
Maprs1057517028
PheGenIrs1057517028
Biobankrs1057517028
1000 genomesrs1057517028
hgdprs1057517028
ensemblrs1057517028
geneviewrs1057517028
scholarrs1057517028
googlers1057517028
pharmgkbrs1057517028
gwascentralrs1057517028
openSNPrs1057517028
23andMers1057517028
SNPshotrs1057517028
SNPdbers1057517028
MSV3drs1057517028
GWAS Ctlgrs1057517028
Max Magnitude0
ClinVar
Risk rs1057517028(A;A)
Alt rs1057517028(A;A)
Reference Rs1057517028(G;G)
Significance Pathogenic
Disease Salla disease not provided
Variation info
Gene SLC17A5
CLNDBN Salla disease not provided
Reversed 1
HGVS NC_000006.11:g.74345104C>T
CLNSRC
CLNACC RCV000412283.1, RCV000437560.1,