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rs786205644

From SNPedia

Orientationplus
Geno Mag Summary
(TGTTGGCCCT;TGTTGGCCCT) 0 common in clinvar
Make rs786205644(-;-)
Make rs786205644(-;TGTTGGCCCT)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position154744559
GeneLRAT
is asnp
is mentioned by
dbSNPrs786205644
ebirs786205644
HLIrs786205644
Exacrs786205644
Varsomers786205644
Maprs786205644
PheGenIrs786205644
hapmaprs786205644
1000 genomesrs786205644
hgdprs786205644
ensemblrs786205644
gopubmedrs786205644
geneviewrs786205644
scholarrs786205644
googlers786205644
pharmgkbrs786205644
gwascentralrs786205644
openSNPrs786205644
23andMers786205644
23andMe allrs786205644
SNP Nexus

SNPshotrs786205644
SNPdbers786205644
MSV3drs786205644
GWAS Ctlgrs786205644
Max Magnitude0
ClinVar
Risk rs786205644(;)
Alt rs786205644(;)
Reference rs786205644(TGTTGGCCCT;TGTTGGCCCT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LRAT
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.155665711_155665720delTGTTGGCCCT
CLNSRC
CLNACC RCV000171516.1,