Have questions? Visit https://www.reddit.com/r/SNPedia

rs397509417

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509417(A;A)
Make rs397509417(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position183701783
GeneTRAPPC11
is asnp
is mentioned by
dbSNPrs397509417
ebirs397509417
HLIrs397509417
Exacrs397509417
Varsomers397509417
Maprs397509417
PheGenIrs397509417
hapmaprs397509417
1000 genomesrs397509417
hgdprs397509417
ensemblrs397509417
gopubmedrs397509417
geneviewrs397509417
scholarrs397509417
googlers397509417
pharmgkbrs397509417
gwascentralrs397509417
openSNPrs397509417
23andMers397509417
23andMe allrs397509417
SNP Nexus

SNPshotrs397509417
SNPdbers397509417
MSV3drs397509417
GWAS Ctlgrs397509417
Max Magnitude0
ClinVar
Risk rs397509417(A;A)
Alt rs397509417(A;A)
Reference rs397509417(G;G)
Significance Pathogenic
Disease Limb-girdle muscular dystrophy
Variation info
Gene TRAPPC11
CLNDBN Limb-girdle muscular dystrophy, type 2S
Reversed 0
HGVS NC_000004.11:g.184622936G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000054408.2,