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rs141387386

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs141387386(G;T)
Make rs141387386(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position41819452
GeneFKBP10
is asnp
is mentioned by
dbSNPrs141387386
ebirs141387386
HLIrs141387386
Exacrs141387386
Varsomers141387386
Maprs141387386
PheGenIrs141387386
hapmaprs141387386
1000 genomesrs141387386
hgdprs141387386
ensemblrs141387386
gopubmedrs141387386
geneviewrs141387386
scholarrs141387386
googlers141387386
pharmgkbrs141387386
gwascentralrs141387386
openSNPrs141387386
23andMers141387386
23andMe allrs141387386
SNP Nexus

SNPshotrs141387386
SNPdbers141387386
MSV3drs141387386
GWAS Ctlgrs141387386
Max Magnitude0
ClinVar
Risk rs141387386(T;T)
Alt rs141387386(T;T)
Reference rs141387386(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FKBP10
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.39975704G>T
CLNSRC
CLNACC RCV000171257.1,