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rs797044884

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044884(-;GA)
Make rs797044884(GA;GA)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position59677130
GeneCLTC
is asnp
is mentioned by
dbSNPrs797044884
dbSNP (old)rs797044884
ClinGenrs797044884
ebirs797044884
HLIrs797044884
Exacrs797044884
Gnomadrs797044884
Varsomers797044884
Maprs797044884
PheGenIrs797044884
Biobankrs797044884
1000 genomesrs797044884
hgdprs797044884
ensemblrs797044884
gopubmedrs797044884
geneviewrs797044884
scholarrs797044884
googlers797044884
pharmgkbrs797044884
gwascentralrs797044884
openSNPrs797044884
23andMers797044884
23andMe allrs797044884
SNP Nexus

SNPshotrs797044884
SNPdbers797044884
MSV3drs797044884
GWAS Ctlgrs797044884
Max Magnitude0
ClinVar
Risk rs797044884(AG;AG)
Alt rs797044884(AG;AG)
Reference Rs797044884(-;-)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene CLTC
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000017.10:g.57754490_57754491dupGA
CLNSRC
CLNACC RCV000190705.1,