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rs527236147

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAA;GAA) 0 common in clinvar
Make rs527236147(-;-)
Make rs527236147(-;GAA)
ReferenceGRCh38 38.1/142
Chromosome11
Position64750423
GenePYGM
is asnp
is mentioned by
dbSNPrs527236147
ebirs527236147
HLIrs527236147
Exacrs527236147
Varsomers527236147
Maprs527236147
PheGenIrs527236147
hapmaprs527236147
1000 genomesrs527236147
hgdprs527236147
ensemblrs527236147
gopubmedrs527236147
geneviewrs527236147
scholarrs527236147
googlers527236147
pharmgkbrs527236147
gwascentralrs527236147
openSNPrs527236147
23andMers527236147
23andMe allrs527236147
SNP Nexus

SNPshotrs527236147
SNPdbers527236147
MSV3drs527236147
GWAS Ctlgrs527236147
Max Magnitude0
ClinVar
Risk rs527236147(;)
Alt rs527236147(;)
Reference rs527236147(GAA;GAA)
Significance Other
Disease Glycogen storage disease
Variation info
Gene PYGM
CLNDBN Glycogen storage disease, type V
Reversed 0
HGVS NC_000011.9:g.64517895_64517897delGAA
CLNSRC ClinVar
CLNACC RCV000128553.4,