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

rs398124185

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398124185(-;-)
Make rs398124185(-;T)
Make rs398124185(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154749031
GeneLRAT
is asnp
is mentioned by
dbSNPrs398124185
ebirs398124185
HLIrs398124185
Exacrs398124185
Varsomers398124185
Maprs398124185
PheGenIrs398124185
hapmaprs398124185
1000 genomesrs398124185
hgdprs398124185
ensemblrs398124185
gopubmedrs398124185
geneviewrs398124185
scholarrs398124185
googlers398124185
pharmgkbrs398124185
gwascentralrs398124185
openSNPrs398124185
23andMers398124185
23andMe allrs398124185
SNP Nexus

SNPshotrs398124185
SNPdbers398124185
MSV3drs398124185
GWAS Ctlgrs398124185
Max Magnitude0
ClinVar
Risk rs398124185(T;T)
Alt rs398124185(T;T)
Reference rs398124185(;)
Significance Pathogenic
Disease not provided
Variation info
Gene LRAT
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.155670183dupT
CLNSRC ClinVar
CLNACC RCV000081184.4,