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rs193302856

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193302856(-;-)
Make rs193302856(-;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position1362612
GeneGNPTG
is asnp
is mentioned by
dbSNPrs193302856
ebirs193302856
HLIrs193302856
Exacrs193302856
Varsomers193302856
Maprs193302856
PheGenIrs193302856
hapmaprs193302856
1000 genomesrs193302856
hgdprs193302856
ensemblrs193302856
gopubmedrs193302856
geneviewrs193302856
scholarrs193302856
googlers193302856
pharmgkbrs193302856
gwascentralrs193302856
openSNPrs193302856
23andMers193302856
23andMe allrs193302856
SNP Nexus

SNPshotrs193302856
SNPdbers193302856
MSV3drs193302856
GWAS Ctlgrs193302856
Max Magnitude0
ClinVar
Risk rs193302856(;)
Alt rs193302856(;)
Reference rs193302856(G;G)
Significance Pathogenic
Disease Mucolipidosis III Gamma
Variation info
Gene GNPTG
CLNDBN Mucolipidosis III Gamma
Reversed 0
HGVS NC_000016.9:g.1412613delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000002929.3,