Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057520111

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520111(C;T)
Make rs1057520111(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position72008083
GeneCHST3
is asnp
is mentioned by
dbSNPrs1057520111
dbSNP (old)rs1057520111
ClinGenrs1057520111
ebirs1057520111
HLIrs1057520111
Exacrs1057520111
Gnomadrs1057520111
Varsomers1057520111
LitVarrs1057520111
Maprs1057520111
PheGenIrs1057520111
Biobankrs1057520111
1000 genomesrs1057520111
hgdprs1057520111
ensemblrs1057520111
gopubmedrs1057520111
geneviewrs1057520111
scholarrs1057520111
googlers1057520111
pharmgkbrs1057520111
gwascentralrs1057520111
openSNPrs1057520111
23andMers1057520111
23andMe allrs1057520111
SNPshotrs1057520111
SNPdbers1057520111
MSV3drs1057520111
GWAS Ctlgrs1057520111
Max Magnitude0
ClinVar
Risk rs1057520111(T;T)
Alt rs1057520111(T;T)
Reference Rs1057520111(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHST3
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.73767841C>T
CLNSRC
CLNACC RCV000437278.1,