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rs104894563

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894563(C;T)
Make rs104894563(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position42911235
GeneG6PC
is asnp
is mentioned by
dbSNPrs104894563
ebirs104894563
HLIrs104894563
Exacrs104894563
Varsomers104894563
Maprs104894563
PheGenIrs104894563
hapmaprs104894563
1000 genomesrs104894563
hgdprs104894563
ensemblrs104894563
gopubmedrs104894563
geneviewrs104894563
scholarrs104894563
googlers104894563
pharmgkbrs104894563
gwascentralrs104894563
openSNPrs104894563
23andMers104894563
23andMe allrs104894563
SNP Nexus

SNPshotrs104894563
SNPdbers104894563
MSV3drs104894563
GWAS Ctlgrs104894563
Max Magnitude0
OMIM232200
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894563(T;T)
Alt rs104894563(T;T)
Reference rs104894563(C;C)
Significance Other
Disease Glycogen storage disease type 1A
Variation info
Gene G6PC
CLNDBN Glycogen storage disease type 1A
Reversed 0
HGVS NC_000017.10:g.41063252C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012779.4,