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rs797044852

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs797044852(-;-)
Make rs797044852(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position41821033
GeneFKBP10
is asnp
is mentioned by
dbSNPrs797044852
ClinGenrs797044852
ebirs797044852
HLIrs797044852
Exacrs797044852
Varsomers797044852
Maprs797044852
PheGenIrs797044852
hapmaprs797044852
1000 genomesrs797044852
hgdprs797044852
ensemblrs797044852
gopubmedrs797044852
geneviewrs797044852
scholarrs797044852
googlers797044852
pharmgkbrs797044852
gwascentralrs797044852
openSNPrs797044852
23andMers797044852
23andMe allrs797044852
SNP Nexus

SNPshotrs797044852
SNPdbers797044852
MSV3drs797044852
GWAS Ctlgrs797044852
Max Magnitude0
ClinVar
Risk rs797044852(-;-)
Alt rs797044852(-;-)
Reference Rs797044852(TG;TG)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene FKBP10
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000017.10:g.39977285_39977286delTG
CLNSRC
CLNACC RCV000190651.1,