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rs769960481

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs769960481(-;-)
Make rs769960481(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position64751627
GenePYGM
is asnp
is mentioned by
dbSNPrs769960481
ebirs769960481
HLIrs769960481
Exacrs769960481
Varsomers769960481
Maprs769960481
PheGenIrs769960481
hapmaprs769960481
1000 genomesrs769960481
hgdprs769960481
ensemblrs769960481
gopubmedrs769960481
geneviewrs769960481
scholarrs769960481
googlers769960481
pharmgkbrs769960481
gwascentralrs769960481
openSNPrs769960481
23andMers769960481
23andMe allrs769960481
SNP Nexus

SNPshotrs769960481
SNPdbers769960481
MSV3drs769960481
GWAS Ctlgrs769960481
Max Magnitude0
ClinVar
Risk rs769960481(;)
Alt rs769960481(;)
Reference rs769960481(A;A)
Significance Probable-Pathogenic
Disease Glycogen storage disease
Variation info
Gene PYGM
CLNDBN Glycogen storage disease, type V
Reversed 0
HGVS NC_000011.9:g.64519099delA
CLNSRC
CLNACC RCV000169141.1,