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rs1058768

From SNPedia

Orientationplus
Stabilizedplus
Make rs1058768(C;C)
Make rs1058768(C;T)
Make rs1058768(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position54321349
GeneTINAG
is asnp
is mentioned by
dbSNPrs1058768
ebirs1058768
HLIrs1058768
Exacrs1058768
Varsomers1058768
Maprs1058768
PheGenIrs1058768
hapmaprs1058768
1000 genomesrs1058768
hgdprs1058768
ensemblrs1058768
gopubmedrs1058768
geneviewrs1058768
scholarrs1058768
googlers1058768
pharmgkbrs1058768
gwascentralrs1058768
openSNPrs1058768
23andMers1058768
23andMe allrs1058768
SNP Nexus

SNPshotrs1058768
SNPdbers1058768
MSV3drs1058768
GWAS Ctlgrs1058768
GMAF0.2498
Max Magnitude
? (C;C) (C;T) (T;T) 28
Venter snp
Source plos
Gene TINAG
allele C
frequency 0.625
sift TOLERATED
HuRef 1103652871600
Disease Association Antibodies against TINAG are found in sera of patients with tubulointerstitial nephritis, a rare autoimmune disorder that causes acute and chronic renal injury.



GET Evidence
TINAG-S158P
aa_change Ser158Pro
aa_change_short S158P
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.701803
summary