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rs119103260

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs119103260(G;G)
Make rs119103260(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position64751970
GenePYGM, RASGRP2
is asnp
is mentioned by
dbSNPrs119103260
ebirs119103260
HLIrs119103260
Exacrs119103260
Varsomers119103260
Maprs119103260
PheGenIrs119103260
hapmaprs119103260
1000 genomesrs119103260
hgdprs119103260
ensemblrs119103260
gopubmedrs119103260
geneviewrs119103260
scholarrs119103260
googlers119103260
pharmgkbrs119103260
gwascentralrs119103260
openSNPrs119103260
23andMers119103260
23andMe allrs119103260
SNP Nexus

SNPshotrs119103260
SNPdbers119103260
MSV3drs119103260
GWAS Ctlgrs119103260
Max Magnitude0
OMIM608455
Desc
Variant0017
Relatedalso
ClinVar
Risk rs119103260(C,G;C,G)
Alt rs119103260(C,G;C,G)
Reference rs119103260(T;T)
Significance Other
Disease Glycogen storage disease
Variation info
Gene PYGM
CLNDBN Glycogen storage disease, type V
Reversed 1
HGVS NC_000011.9:g.64519442A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002404.5,