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

rs143023066

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs143023066(C;T)
Make rs143023066(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position49440273
GeneMUT
is asnp
is mentioned by
dbSNPrs143023066
dbSNP (old)rs143023066
ClinGenrs143023066
ebirs143023066
HLIrs143023066
Exacrs143023066
Gnomadrs143023066
Varsomers143023066
LitVarrs143023066
Maprs143023066
PheGenIrs143023066
Biobankrs143023066
1000 genomesrs143023066
hgdprs143023066
ensemblrs143023066
gopubmedrs143023066
geneviewrs143023066
scholarrs143023066
googlers143023066
pharmgkbrs143023066
gwascentralrs143023066
openSNPrs143023066
23andMers143023066
23andMe allrs143023066
SNPshotrs143023066
SNPdbers143023066
MSV3drs143023066
GWAS Ctlgrs143023066
Max Magnitude0
ClinVar
Risk rs143023066(T;T)
Alt rs143023066(T;T)
Reference Rs143023066(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MUT
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.49407986C>T
CLNSRC
CLNACC RCV000489642.1,