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rs119103256

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs119103256(C;G)
Make rs119103256(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position64750557
GenePYGM, RASGRP2
is asnp
is mentioned by
dbSNPrs119103256
ebirs119103256
HLIrs119103256
Exacrs119103256
Varsomers119103256
Maprs119103256
PheGenIrs119103256
hapmaprs119103256
1000 genomesrs119103256
hgdprs119103256
ensemblrs119103256
gopubmedrs119103256
geneviewrs119103256
scholarrs119103256
googlers119103256
pharmgkbrs119103256
gwascentralrs119103256
openSNPrs119103256
23andMers119103256
23andMe allrs119103256
SNP Nexus

SNPshotrs119103256
SNPdbers119103256
MSV3drs119103256
GWAS Ctlgrs119103256
Max Magnitude0
OMIM608455
Desc
Variant0010
Relatedalso
ClinVar
Risk rs119103256(G;G)
Alt rs119103256(G;G)
Reference rs119103256(C;C)
Significance Pathogenic
Disease Glycogen storage disease
Variation info
Gene PYGM
CLNDBN Glycogen storage disease, type V
Reversed 1
HGVS NC_000011.9:g.64518029G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002393.3,