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rs879253779

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs879253779(A;G)
Make rs879253779(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position184072258
GeneTSEN15
is asnp
is mentioned by
dbSNPrs879253779
ebirs879253779
HLIrs879253779
Exacrs879253779
Varsomers879253779
Maprs879253779
PheGenIrs879253779
hapmaprs879253779
1000 genomesrs879253779
hgdprs879253779
ensemblrs879253779
gopubmedrs879253779
geneviewrs879253779
scholarrs879253779
googlers879253779
pharmgkbrs879253779
gwascentralrs879253779
openSNPrs879253779
23andMers879253779
23andMe allrs879253779
SNP Nexus

SNPshotrs879253779
SNPdbers879253779
MSV3drs879253779
GWAS Ctlgrs879253779
Max Magnitude0
ClinVar
Risk rs879253779(G;G)
Alt rs879253779(G;G)
Reference rs879253779(A;A)
Significance Pathogenic
Disease Pontocerebellar hypoplasia
Variation info
Gene TSEN15
CLNDBN Pontocerebellar hypoplasia, type 2f
Reversed 0
HGVS NC_000001.10:g.184041392A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000234975.1,